FDA Inspection 1045668 — AptaPharma Inc.

AptaPharma Inc. — FEI 3010164738

The FDA completed an inspection of AptaPharma Inc. on Mar 16, 2018 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). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 16, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Pennsauken, NJ (United States)

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