News Detail
Maryland, 17 April 2024: The FDA slammed three Indian drugmakers with Form 483s following recent inspections that uncovered unsanitary conditions, broken equipment and poor recordkeeping.
Mumbai-based Alkem Labs was cited with View Details
Source : Fierce Pharma
FDA
Form 483
Cipla
Alkem Laboratories
Zydus Cadila
quality control
Asia
Manufacturing
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