USFDA indicates voluntary action for Aurobindo Pharma: AP

The U.S. regulator conducted an inspection of unit XIV from May 15 to 19, 2023.

235
USFDA Inspection
USFDA Inspection

Last Updated on October 10, 2024 by The Health Master

Hyderabad: Aurobindo Pharma has received an Establishment Inspection Report (EIR) from the US Food and Drug Administration (USFDA) for Unit XIV located at Bonangi Village, Jawaharlal Nehru Pharma City, Parawada Mandal, Anakapalli District, Andhra Pradesh.

The U.S. regulator conducted an inspection of unit XIV from May 15 to 19, 2023.

“The Unit has now received the Establishment Inspection Report classifying the facility as “Voluntary action indicated” (VAI),’‘ the Hyderabad-based company informed the BSE on Monday. 

The exact details of VAI have not been disclosed. 

USFDA issues Form 483 with one observation to Gland Pharma: Hyderabad

USFDA issues Form 483 to Lupin with 2 observations: Nagpur

USFDA completes inspection of Granules India in two facilities

USFDA completes inspection at Ajanta Pharma with zero observations: Gujarat

USFDA concludes inspection at Zydus with zero observation

USFDA completes inspection of Dr Reddy’s with zero observation

For informative videos by The Health Master, click on the below YouTube icon:

YouTube Icon

For informative videos on Medical Store / Pharmacy, click on the below YouTube icon:

YouTube Icon

For informative videos on the news regarding Pharma / Medical Devices / Cosmetics / Homoeopathy etc., click on the below YouTube icon:

YouTube Icon

For informative videos on consumer awareness, click on the below YouTube icon:

YouTube Icon
Telegram
WhatsApp
Facebook
LinkedIn
YouTube Icon
Google-news