FDA inspection
GETSCH+HILLER MEDIZINTECHNIK GmbH: FDA inspection ending Jul 21, 2022
FDA inspection 1177939 · Official Action Indicated (OAI) · Tuttlingen
Key facts
| Inspection ID | 1177939 |
|---|---|
| Firm | GETSCH+HILLER MEDIZINTECHNIK GmbH |
| FEI number | 3008911114 |
| Address | Sattlerstr. 20 |
| City | Tuttlingen |
| Country | Germany |
| Fiscal year | 2022 |
| Inspection end date | Jul 21, 2022 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
| Warning letter | 644680 |
At a glance
- None 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