"Laurus Labs Limited has received the Establishment Inspection Report (EIR) from USFDA for its unit 1 and 3, located at Parawada, Visakhapatnam, for the inspection conducted in August 2017," the drug maker said in a statement.
The company had earlier said that the US regulator completed the inspection with two observations which were in " procedural in nature".
The city-based pharma company had also said it was a regular surveillance audit by the USFDA and no data integrity issues were observed.
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