Unichem Labs Pithampur facility gets USFDA EIR

Written By :  Ruchika Sharma
Medically Reviewed By :  Dr. Kamal Kant Kohli
Published On 2025-05-14 12:09 GMT   |   Update On 2025-05-14 12:09 GMT

Mumbai: Unichem Labs has announced that United States Food and Drug Administration (USFDA) has classified the inspection at the Company's Pithampur API facility as Voluntary Action Initiated ("VAI") and issued the Establishment Inspection Report (EIR).

The facility was inspected from 24th February 2025 to 28th February 2025. In March, the facility had initially received four observations from the USFDA.

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Read also: Unichem Labs Pithampur API facility gets 4 USFDA observations

Voluntary Action Indicated (VAI) classification indicates the inspection found objectionable conditions or practices but the agency has determined the facility can voluntarily correct its deficiencies and will not recommend any action.

Headquartered in Mumbai, Unichem Laboratories Limited is an international, integrated, specialty pharmaceutical company. The company was founded in 1944 by Padmabhushan Late Mr. Amrut V Mody. It manufactures and markets a large basket of pharmaceutical formulations as branded generics as well as generics in several markets across the world.

Read also: Sandip Ghume to resign as Unichem Labs Deputy CFO, Key Managerial Personnel



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