"United States Food and Drug Administration (USFDA) recently concluded audit of our three manufacturing facilities in Goa and has issued four observations across these three facilities," Cipla said in a filing to BSE.
These observations were primarily procedural in nature and the company has already responded to the same, it added.
The company, however, did not provide any details of the observations.
"We continue to operate our facilities with a high level of compliance and control," Cipla said.
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