FDA Warning Letter — Derma Pen, LLC

Case 437705 — FEI 3009081613

The FDA took a Warning Letter action against Derma Pen, LLC on January 9, 2015 (Salt Lake City, UT). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Derma Pen, LLC
Date
January 9, 2015
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Salt Lake City, UT (United States)