Source: FDA, document on fileFDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it.
To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3011905047.
Eugia SEZ Private Limited
Mahabubnagar District, -, India
Issue DateMarch 01, 2019
FEI Number3011905047
CountryIndia
Status
No Warning Letter
Product Type
Drugs
Establishment Type
Finished Pharmaceutical Manufacturer
Sub Systems Impacted
11
Batch ManufacturingComputer System ValidationContamination ControlEnvironmental MonitoringInvestigationsLaboratory ControlsMaterial Sampling and TestingProcess ControlQuality Risk ManagementSample TestingTraining Management
