FDA Warning Letter — Transdermal Cap Inc.

Case 475751 — FEI 3008699663

The FDA took a Warning Letter action against Transdermal Cap Inc. on Aug 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
Aug 10, 2015
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Highland Heights, OH (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.