FDA Inspection 1220102 — Smilax Laboratories Limited

Smilax Laboratories Limited — FEI 3008772334

The FDA completed an inspection of Smilax Laboratories Limited on September 15, 2023 in Parawada- Vishakapatnam District. 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 15, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Parawada- Vishakapatnam District (India)