FDA Inspection 1331256 — AptaPharma Inc.

AptaPharma Inc. — FEI 3010164738

The FDA completed an inspection of AptaPharma Inc. on Aug 14, 2026 in Pennsauken, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 14, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Pennsauken, NJ (United States)

Citations

IDCFRDescription
192021 CFR 211.166(a)(3)Valid stability test methods
360321 CFR 211.160(b)Scientifically sound laboratory controls

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