FDA Inspection 1287532 — 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 Sep 5, 2025 in Mirfield. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 5, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mirfield (United Kingdom)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.