FDA Warning Letter — Aspire Pharmaceuticals, Inc.

Case 630105 — FEI 3003159106

The FDA took a Warning Letter action against Aspire Pharmaceuticals, Inc. on November 22, 2022 (Somerset, 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
Aspire Pharmaceuticals, Inc.
Date
November 22, 2022
Fiscal Year
2023
Product Type
Drugs
Center
CDER
Location
Somerset, NJ (United States)