483
Aarti Pharmalabs LimitedAarti Pharmalabs Limited – FDA 483, Feb 20, 2020
Record Details
Aarti Industries Limited, an API manufacturer in Palghar, India, was cited for four observations during an FDA inspection. The inspection revealed issues including insecure storage of quality control samples, incomplete investigations into out-of-specification results, unapproved raw material dispensing and collection bags, and poor documentation practices in sample receiving logs. These deficiencies indicate a lack of adherence to established quality standards and procedures.
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