Laurus Labs Limited today said it received Establishment Inspection Report (EIR) from the US Food and Drug Administration(USFDA) for its API (active pharma ingredients) plants located at Visakhapatnam in Andhra Pradesh.
"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.
(This story has not been edited by Business Standard staff and is auto-generated from a syndicated feed.)