FDA Warning Letter — Aurolife Pharma, LLC

Case 607087 — FEI 3005796917

The FDA took a Warning Letter action against Aurolife Pharma, LLC on October 16, 2020 (Dayton, NJ). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Aurolife Pharma, LLC
Date
October 16, 2020
Fiscal Year
2021
Product Type
Drugs
Center
CDER
Location
Dayton, NJ (United States)