Kevin Morin, Debra Morin, and Amy Harris
Morin Enterprises Inc. d/b/a Ecig Crib
3027 Coon Rapids Blvd. NW
Coon Rapids , MN 55433
United States
ecigcribcsr@gmail.com
(b)(6)FEI 3013889341Issued Mar 26, 2021Center for Tobacco Products
Source: FDA, published letter. FDA published this warning letter; View Letter opens FDA's copy. To check it, open FDA's record for this establishment, listed under FEI 3013889341.
Violations1
Issue DateMar 26, 2021
Product TypeTobacco
StatusOpen
Letter Details
Firm
Morin Enterprises Inc. d/b/a Ecig Crib
Location
Kevin Morin, Debra Morin, and Amy Harris
Morin Enterprises Inc. d/b/a Ecig Crib
3027 Coon Rapids Blvd. NW
Coon Rapids , MN 55433
United States
ecigcribcsr@gmail.com
(b)(6)
FEI Number
3013889341
Country
United States
Issue Date
March 26, 2021
Issuing Office
Center for Tobacco Products
Product Type
Tobacco
Status
Open
Summary
Morin Enterprises Inc. d/b/a Ecig Crib was warned for manufacturing and selling e-liquid tobacco products without required premarket authorization. The FDA determined that the company's e-liquids, offered for sale through their website ecigcrib.com, qualified as newly deemed tobacco products subject to FDA jurisdiction under the Family Smoking Prevention and Tobacco Control Act but lacked the mandated premarket marketing authorization orders required for legal sale in the United States. The violation centered on the company's failure to comply with new tobacco product registration requirements that have been in effect since the August 8, 2016 deeming rule.
Morin Enterprises Inc. d/b/a Ecig Crib FDA Warning Letter, March 26, 2021
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