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FDA Inspection 947721 — Synthimed Labs Private Limited

Synthimed Labs Private Limited — FEI 3005895238

The FDA completed an inspection of Synthimed Labs Private Limited on November 6, 2015 in Mohali. 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
November 6, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mohali (India)

Facility

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FDA data resources