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# Dr. Reddy’s Form 483 Posted on Bachupally, India Inspection
- URL: https://www.fdaweb.com/dr-reddys-form-483-posted-on-bachupally-india-inspection/
- Published: 2017-05-05T12:00:00.000Z
- Updated: 2026-09-14T22:21:58.000Z
- Author: David McFarland
- Tags: Drugs, #legacy-id-D5138630

FDA has posted a Dr. Reddy’s Laboratories [Form 483](https://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/CDERFOIAElectronicReadingRoom/UCM556770.pdf?ref=fdaweb.com) from a 4/28 inspection that cited the firm’s Bachupally, Hyderabad, India manufacturing facility on 11 observations. The agency said the firm’s lab controls do not include scientifically sound and appropriate sampling plans. It also found that the lab records are deficient in that they do not include a complete record of all data obtained during testing.