FDA Inspection 1288012 — Arch Pharmalabs Limited

Arch Pharmalabs Limited — FEI 3002808114

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.