FDA Warning Letter — Arnold Professional Pharmacy

Case 521908 — FEI 3012283530

The FDA took a Warning Letter action against Arnold Professional Pharmacy on Apr 7, 2017 (Arnold, MD). The action was issued by CDER and concerns drugs products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Arnold Professional Pharmacy
Date
Apr 7, 2017
Fiscal Year
2017
Product Type
Drugs
Center
CDER
Location
Arnold, MD (United States)