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483
•Dr. Reddy's Laboratories Limited•May 24, 2025

Dr. Reddy's Laboratories Limited – FDA 483, May 24, 2025

Record Details

An FDA inspection of Dr. Reddy's Laboratories Limited – CTO 5, an API manufacturer in Telangana, India, revealed two significant observations. The firm failed to ensure equipment surfaces were maintained in good repair, as a streak was found on a reactor after line clearance and was not recorded. Additionally, electronic batch records were deficient, showing identical date and time stamps for both first and second person reviews, indicating a lack of proper documentation for quality-related activities.

Company
Dr. Reddy's Laboratories Limited
Inspection date
May 24, 2025
Product type
drugs
Office
Office of Inspections and Investigations
Person
  • Santos E. Camara
View Company Profile

ID · b2f49475-3e13-4ffc-ab5d-d0c60fb7bf75

Other documents for Dr. Reddy's Laboratories Limited
  • 483 - 2020-03-05March 5, 2020
  • 483 - 2017-02-21February 21, 2017
  • CRL
  • CRL

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