USFDA successfully concludes inspection at Neuland Labs Bonthapally facility
Written By : Ruchika Sharma
Medically Reviewed By : Dr. Kamal Kant Kohli
Published On 2024-03-22 11:01 GMT | Update On 2024-03-22 11:01 GMT
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Hyderabad: Neuland Laboratories Limited has announced that the United States Food and Drug Administration (US FDA) has successfully completed the inspection at the Company's Unit 1 manufacturing facility at Bonthapally, Hyderabad with no observations under Form 483.
The facility was inspected from 18th to 22nd of March 2024.
"We wish to inform you that the United States Food and Drug Administration (“US FDA”) has inspected our Unit 1 manufacturing facility at Bonthapally, Hyderabad from 18th to 22nd of March 2024. The inspection at Unit 1 by the US FDA has been successfully completed, with no observations under Form 483," the Company stated in a BSE filing.
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