FDA Inspection 1044760 — Synthimed Labs Private Limited

Synthimed Labs Private Limited — FEI 3005895238

The FDA completed an inspection of Synthimed Labs Private Limited on March 16, 2018 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
March 16, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mohali (India)