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USFDA inspection: Ipca Labs Piparia facility gets VAI status
Mumbai: Ipca Labs has announced that the United States Food and Drug Administration (USFDA) has determined the inspection classification of the Piparia (Silvassa) formulations manufacturing facility as Voluntary Action Indicated (VAI). The USFDA had inspected the said facility from 18th April, 2023 to 26th April, 2023 and issued three observations under USFDA Form 483.Read also: Ipca Labs gets...
Mumbai: Ipca Labs has announced that the United States Food and Drug Administration (USFDA) has determined the inspection classification of the Piparia (Silvassa) formulations manufacturing facility as Voluntary Action Indicated (VAI).
Voluntary action indicated (VAI) means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
Ipca Laboratories Limited is an Indian multinational pharmaceutical company headquartered in Mumbai. The Company was founded by group of businessmen and medical professionals in 1949. It produces theobromine, acetyl thiophene, and p-bromotoluene as active pharmaceutical ingredients (APIs). Ipca sells these APIs and their intermediates globally. Ipca is a fully-integrated pharmaceutical company that manufactures over 350 formulations and 80 APIs for various therapeutic segments.
Ruchika Sharma joined Medical Dialogue as an Desk Editor for the Business Section in 2019. She covers all the updates in the Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She has completed her B.Com from Delhi University and then pursued postgraduation in M.Com. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751