The FDA Just Cleared Up Some Things

vape shop

The FDA has announced that is will allow vaporizer shops to change coils, assemble kits, and refill tanks on site for customers without being designated tobacco products manufacturers under the current regulations.

The FDA has just issued guidance on the rule, for the first time spelling out for anyone to understand what activities are allowed to happen in retail stores. Since the current regulations were published, business owners have tried repeatedly to get this information to be in compliance. Many vapor retailers have interpreted the regulations to include prohibition of basic customer service activities.

The current ruling was issued last May, and took effect on August 8, 2016. According to the FDA, any retail business that “creates or modifies” one of the newly deemed “tobacco products” is considered a manufacturer, and is required to register as a manufacturer and list all products they sell, submit health documents to the agency, report ingredient lists, and report harmful and potentially harmful components. Additionally, manufacturers are required to submit premarket tobacco applications for all products they create or modify. What a nightmare this creates.

Many vapor retailers have interpreted the regulations to include prohibition of basic customer service activities like changing coils, assembling a device from a kit for a new vaper, performing simple repairs, or explaining product properly functions. The FDA has avoided explaining exactly what is allowed during many attempt with shop owners seeking clarifications.

The following activities can be done without qualifying the vape shop as a manufacturer:

  • “Demonstrating or explaining the use of an ENDS product without assembling the product”
  • “Maintaining an ENDS product by cleaning or tightening fixtures (e.g., screws)”
  • “Replacing coils in an ENDS product with identical coils (e.g., same ohm and wattage rating)”
  • “Assembling a final product from the components and parts packaged together in an ENDS kit”

Additionally, the FDA says it will not enforce some activities that it does classify as “modifying” deemed products. According to its announcement, the FDA “does not intend to enforce the five requirements listed above for these vape shops if, generally speaking, all modifications are consistent with the conditions of the FDA marketing authorization (MA) or if the original manufacturer provides specifications and all modifications made are consistent with those specifications.”

Examples of modifications the FDA will now allow include:

  • “Refilling an open system ENDS if no further modifications are made to the device or to the e-liquid before, during or after the refill that are outside the FDA marketing authorization (MA) order”
  • “Refilling an open ENDS system if no further modifications are made to the device or the e-liquid before, during or after the refill that – if there is no MA order – are inconsistent with the manufacturer’s specifications”

In other words, they will allow vaporizer shops to help a customer refill a tank, as long as no modifications are made to the device aside from what is recommended by the manufacturer in their info and marketing materials.

They specifically explain that replacing coils with anything other than stock coils designed for a particular atomizer is prohibited. So, no building by shop employees for customers is allowed at all. Filling a closed-system device is also specifically prohibited. So if you’re an expert at hacking sealed pods… Don’t do it for customers in your store.

The publication of the new draft guidance also opens a brief window for public comment. All retailers and customers of vape shops can offer specific criticism or advice on how the deeming rule affects transactions in vape shops. Comments can be made at the site, under Docket No. FDA-2017-D-0120

The draft guidance closely follows two deadlines for manufacturers being postponed by the FDA. The due date for manufacturers to register with the agency was pushed back from December 31, 2016 to June 30, 2017. Soon after that, the FDA also delayed the deadline for submitting ingredient listings from Feb. 8 to Aug. 8, 2017.

Lastly, the agency announces in this document that it will not enforce the requirement that all tobacco products “include an accurate statement of the percentage of foreign and domestic-grown tobacco used in the products.”

It sure if nice to have some of this info to put vape shops minds at ease as at least it is not a guessing game anymore.

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