Warning letter
DRG Instruments GmbH: warning letter of Sep 19, 2017
FDA warning letter 522669 · Center for Devices and Radiological Health
Key facts
| Reference number | 522669 |
|---|---|
| Company | DRG Instruments GmbH |
| Subject | CGMP/QSR/Medical Devices/Adulterated |
| Issue date | Sep 19, 2017 |
| Posted date | Sep 19, 2017 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| CFR sections cited | 807.81(a)(3)(i), 807.81(b), 806, 806.10, 806.2(j), 820 |
| Inspection city | Marburg |
| Inspection start date | Oct 24, 2016 |
| Letter on fda.gov | fda.gov |
At a glance
- 1–9 CFR sections cited
- OAI Linked inspection classification
- Yes Form FDA 483 issued
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA warning letters
FDA warning letters notify a firm of significant regulatory violations found during an inspection or review and request prompt corrective action.
Source: U.S. Food and Drug Administration (FDA), Warning Letters · Source date: