FDA Warning Letter — A.P. Deauville, LLC

Case 586306 — FEI 3004007943

The FDA took a Warning Letter action against A.P. Deauville, LLC on Nov 8, 2019 (Easton, 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
A.P. Deauville, LLC
Date
Nov 8, 2019
Fiscal Year
2020
Product Type
Drugs
Center
CDER
Location
Easton, PA (United States)

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