Result after a FDA-inspection; reports are classified as NAI (no action indicated) = the investigator is in compliance, VAI-1 (voluntary action indicated) = objectionable condition or practice was corrected during the inspection and the conditions had minimal effect on the integrity (validity of ...
Somerset, NJ, Mumbai, July 07, 2022: Global pharma major Lupin Limited (Lupin) today announced that it has received the Establishment Inspection Report (EIR) from United States Food and Drug Administration (US FDA) for its Somerset, NJ manufacturing facility, after the inspection of the facility...
Cipla Ltd has received Establishment Inspection Report (EIR) from United States Food and Drug Administration (FDA) for Patalganga manufacturing facility in Maharashtra.The company announced the closure of inspection by the US FDA at its Patalganga manufacturing facility."The inspection was carried out...
Dr Reddy's Laboratories has received an establishment inspection report (EIR) from the US health regulator after audit of its UK facility
эиргенфармалтд eirgen pharma ltd. is AOther Supplier. This Company's Trade Report Mainly Contains Market Analysis, Contact, Trade Partners, Ports Statistics, And Trade Area Analysis. Official Reference Contact Is From Other Original Bill Of Ladings, Including Email, Phone, Fax...