FDA Inspection 1045668 — AptaPharma Inc.

AptaPharma Inc. — FEI 3010164738

The FDA completed an inspection of AptaPharma Inc. on March 16, 2018 in Pennsauken, 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
March 16, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Pennsauken, NJ (United States)