FDA Inspection 1313542 — Symbiotec Pharmalab Limited

Symbiotec Pharmalab Limited — FEI 3005122933

The FDA completed an inspection of Symbiotec Pharmalab Limited on Apr 3, 2026 in Mhow. 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
Apr 3, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mhow (India)

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