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 Jun 16, 2017 in Srikakulam. 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
Jun 16, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Srikakulam (India)

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