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USFDA issues one observation for Unichem's Ghaziabad formulations facility

"The United States Food and Drug Administration (USFDA) conducted inspection at the company's Ghaziabad formulation facility between August 19, 2019 to August 23, 2019. The inspection was a routine Good manufacturing practice (GMP) surveillance," Unichem said in a regulatory filing.

August 26, 2019 / 11:24 AM IST
 
 
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Drug firm Unichem Laboratories on Monday said the US health regulator has issued one observation after the inspection of its formulations facility at Ghaziabad.

"The United States Food and Drug Administration (USFDA) conducted inspection at the company's Ghaziabad formulation facility between August 19, 2019 to August 23, 2019. The inspection was a routine Good manufacturing practice (GMP) surveillance," Unichem said in a regulatory filing.

"At the end of inspection, the facility received one observation which is not a repeat observation and is procedural in nature," the company added.

Unichem said it will provide the response and corrective action plan within next 15 working days to address the USFDA observation.

Shares of Unichem Laboratories were trading 1.45 percent lower at Rs 235.20 apiece on BSE.

PTI
first published: Aug 26, 2019 11:18 am

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