FDA Warning Letter — Transdermal Cap Inc.

Case 475751 — FEI 3008699663

The FDA took a Warning Letter action against Transdermal Cap Inc. on August 10, 2015 (Highland Heights, OH). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Transdermal Cap Inc.
Date
August 10, 2015
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Highland Heights, OH (United States)