FDA Inspection 1214674 — Aspire Pharmaceuticals, Inc.

Aspire Pharmaceuticals, Inc. — FEI 3003159106

The FDA completed an inspection of Aspire Pharmaceuticals, Inc. on July 14, 2023 in Somerset, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 14, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Somerset, NJ (United States)