FDA inspection
Aurobindo Pharma Limited - Unit IV: FDA inspection ending Nov 13, 2019
FDA inspection 1109604 · Voluntary Action Indicated (VAI) · Medak District, Hyderabad
Key facts
| Inspection ID | 1109604 |
|---|---|
| Firm | Aurobindo Pharma Limited - Unit IV |
| FEI number | 3008461619 |
| Address | Plot Nos. 4, 34 To 48, Epip, Tsiic, Ida, Pashamylaram, Patancheru Mandal, Sangareddy |
| City | Medak District, Hyderabad |
| Fiscal year | 2020 |
| Inspection end date | Nov 13, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med 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Evaluation|Compliance: Medical Devices|Drug Quality Assurance|Generic Drug Evaluation |
| Product type | Devices, Drugs |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data