FDA inspection
Remel Inc.: FDA inspection ending Apr 12, 2017
FDA inspection 1009751 · Voluntary Action Indicated (VAI) · Oakwood Village, OH
Key facts
| Inspection ID | 1009751 |
|---|---|
| Firm | Remel Inc. |
| FEI number | 1000515493 |
| Address | 1 Thermo Fisher Way |
| City | Oakwood Village |
| State | OH |
| ZIP | 44146 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Apr 12, 2017 |
| 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
- 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