FDA Inspection 1293102 — Apertus Pharmaceuticals

Apertus Pharmaceuticals — FEI 3010401502

The FDA completed an inspection of Apertus Pharmaceuticals on October 31, 2025 in Ballwin, MO. 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
October 31, 2025
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ballwin, MO (United States)