FDA Warning Letter — Coupler LLC

Case 607662 — FEI 3003734940

The FDA took a Warning Letter action against Coupler LLC on Sep 15, 2020 (West Chester, PA). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Coupler LLC
Date
Sep 15, 2020
Fiscal Year
2020
Product Type
Drugs
Center
CDER
Location
West Chester, PA (United States)

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