News
The inspection by the U.S. Food and Drug Administration (FDA) focused on the company's active pharmaceutical ingredients (API ...
Dr Reddy's Laboratories (DRL) said that US Food and Drug Administration (USFDA) had conducted a GMP inspection at its API Middleburgh facility in New York, USA from 12th May to 16th May 2025.
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback