FDA Inspection 1095657 — Dr. Reddy's Laboratories Ltd.

Dr. Reddy's Laboratories Ltd. — FEI 3006549835

The FDA completed an inspection of Dr. Reddy's Laboratories Ltd. on June 21, 2019 in Visakhapatnam. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 21, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Visakhapatnam (India)