FDA inspection
Dimequip: FDA inspection ending Apr 28, 2000
FDA inspection 24056 · Official Action Indicated (OAI) · Frameries
Key facts
| Inspection ID | 24056 |
|---|---|
| Firm | Dimequip |
| FEI number | 3002808467 |
| Address | Route De Bavay |
| City | Frameries |
| Fiscal year | 2000 |
| Inspection end date | Apr 28, 2000 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
| Warning letter | UCM068564 |
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