FDA inspection
Gebruder Brasseler GmbH & Co. KG: FDA inspection ending Feb 18, 2000
FDA inspection 18560 · Voluntary Action Indicated (VAI) · Lemgo
Key facts
| Inspection ID | 18560 |
|---|---|
| Firm | Gebruder Brasseler GmbH & Co. KG |
| FEI number | 3002806577 |
| Address | Trophagener Weg 25, Postfach 160 |
| City | Lemgo |
| Fiscal year | 2000 |
| Inspection end date | Feb 18, 2000 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None 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