FDA inspection
Philips India Limited: FDA inspection ending Sep 25, 2019
FDA inspection 1122759 · Voluntary Action Indicated (VAI) · Chakan
Key facts
| Inspection ID | 1122759 |
|---|---|
| Firm | Philips India Limited |
| FEI number | 3010685285 |
| Address | Plot No B - 79, Midc; Phase - Ii |
| City | Chakan |
| Fiscal year | 2019 |
| Inspection end date | Sep 25, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Medical Devices |
| Product type | Devices |
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