FDA inspection
Systagenix Wound Management Manufacturing, Ltd: FDA inspection ending Jan 18, 2024
FDA inspection 1230384 · Voluntary Action Indicated (VAI) · Skipton
Key facts
| Inspection ID | 1230384 |
|---|---|
| Firm | Systagenix Wound Management Manufacturing, Ltd |
| FEI number | 3007663067 |
| Address | Airebank Mills |
| City | Skipton |
| Country | United Kingdom |
| Fiscal year | 2024 |
| Inspection end date | Jan 18, 2024 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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