US FDA issues warning letter to Glenmark for its Baddi facility
US FDA had inspected the facility between April 15 and April 20 and earlier classified the inspection as an official action…
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Warning Letter
Lupin gets warning letter from US FDA for Mandideep facility
Lupin said there are no drug master file and abbreviated new drug applications (ANDA) pending review or approval from the…
Indoco’s Goa Plant I receives Warning Letter from US FDA
The facility had received six observations in Form 483s and was classified as ‘OAI’ (Official Action Indicated’) in March 2019