FDA Inspection 1119807 — Dr. Reddy's Laboratories (EU) Ltd.

Dr. Reddy's Laboratories (EU) Ltd. — FEI 3002807544

The FDA completed an inspection of Dr. Reddy's Laboratories (EU) Ltd. on October 24, 2019 in Mirfield. 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
October 24, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mirfield (United Kingdom)

Additional Details

Mutual Recognition Agreement (MRA)