homehealthcare NewsIPCA Laboratories' Ratlam facility gets favourable FDA classification

IPCA Laboratories' Ratlam facility gets favourable FDA classification

The US FDA has classified IPCA Laboratories' Ratlam facility, which manufactures API's, as ‘Voluntary Action Indicated’ (VAI)in its Establishment Inspection Report (EIR). A VAI is generally issued when the response from a plant to certain observations appears satisfactory to the regulator.

By Ekta Batra  Oct 23, 2023 5:18:08 PM IST (Published)

2 Min Read
IPCA Laboratories has received a clean chit for its Ratlam manufacturing unit from the US Food and Drug Administration (USFDA).
FDA classified the Ratlam facility, which specialises in manufacturing Active Pharmaceutical Ingredients (APIs), as 'Voluntary Action Indicated' (VAI) in its Establishment Inspection Report (EIR).
VAI is the second-best classification that a plant can get from the USFDA. The classification, as defined by the regulator, is as follows: ‘Objectionable conditions or practices were found during the inspection but the agency is not prepared to take or recommend any administrative or regulatory action’.