FDA inspection
Centurion Medical Products, LP: FDA inspection ending Aug 20, 2019
FDA inspection 1100169 · Official Action Indicated (OAI) · Howell, MI
Key facts
| Inspection ID | 1100169 |
|---|---|
| Firm | Centurion Medical Products, LP |
| FEI number | 1824619 |
| Address | 301 Catrell Dr |
| City | Howell |
| State | MI |
| ZIP | 48843 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Aug 20, 2019 |
| Classification | Official Action Indicated (OAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
| Warning letter | 598837 |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- Yes 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