FDA inspection
Philips Medical Systems (Cleveland) Inc: FDA inspection ending Aug 18, 2017
FDA inspection 1022578 · Official Action Indicated (OAI) · Cleveland, OH
Key facts
| Inspection ID | 1022578 |
|---|---|
| Firm | Philips Medical Systems (Cleveland) Inc |
| FEI number | 1525965 |
| Address | 595 Miner Rd |
| City | Cleveland |
| State | OH |
| ZIP | 44143 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Aug 18, 2017 |
| Classification | Official Action Indicated (OAI) |
| 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
- No Establishment inspection report (EIR) exists
- 10–99 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