Dr Reddy's Labs gets 2 USFDA observations for Duvvada facilities
Written By : Ruchika Sharma
Medically Reviewed By : Dr. Kamal Kant Kohli
Published On 2024-05-18 06:00 GMT | Update On 2024-05-18 06:00 GMT
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Hyderabad: Dr Reddy's Labs has informed in a recent BSE filing, that the United States Food & Drug Administration (USFDA) has concluded a routine GMP inspection with two observations at the Company's formulations manufacturing facilities (FTO-7 & FTO-9) in Duvvada, Visakhapatnam.
The inspection was conducted from 8th May to 17th May, 2024.
"We have been issued a Form 483 with two observations, which we will address within the stipulated timeline," the Company stated in a BSE filing.
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