FDA Inspection 1288012 — Arch Pharmalabs Ltd.

Arch Pharmalabs Ltd. — FEI 3002808114

The FDA completed an inspection of Arch Pharmalabs Ltd. on September 12, 2025 in Dombivli. 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
September 12, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dombivli (India)