FDA inspection
Degania Medical Devices Pvt. Ltd.: FDA inspection ending Jan 21, 2016
FDA inspection 959093 · Voluntary Action Indicated (VAI) · Gurgaon
Key facts
| Inspection ID | 959093 |
|---|---|
| Firm | Degania Medical Devices Pvt. Ltd. |
| FEI number | 3005483737 |
| Address | Plot No 251, Imt Manesar |
| City | Gurgaon |
| Country | India |
| Fiscal year | 2016 |
| Inspection end date | Jan 21, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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