FDA inspection
DRG Instruments GmbH: FDA inspection ending Oct 28, 2016
FDA inspection 999374 · Official Action Indicated (OAI) · Marburg
Key facts
| Inspection ID | 999374 |
|---|---|
| Firm | DRG Instruments GmbH |
| FEI number | 3002800697 |
| Address | Frauenbergstr. 18 |
| City | Marburg |
| Country | Germany |
| Fiscal year | 2017 |
| Inspection end date | Oct 28, 2016 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
| Warning letter | 522669 |
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
- 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