FDA Inspection 1005458 — Dr. Reddy's Laboratories Limited

Dr. Reddy's Laboratories Limited — FEI 3005447965

The FDA completed an inspection of Dr. Reddy's Laboratories Limited on Feb 21, 2017 in Nalgonda. 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
Feb 21, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Nalgonda (India)

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