FDA Inspection 1018229 — Dr Reddy's Laboratories Limited

Dr Reddy's Laboratories Limited — FEI 3009193040

The FDA completed an inspection of Dr Reddy's Laboratories Limited on June 16, 2017 in Srikakulam. 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
June 16, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Srikakulam (India)