FDA inspection
Aesculap-Chifa SP. Z.O.O.: FDA inspection ending Dec 11, 2003
FDA inspection 305076 · Voluntary Action Indicated (VAI) · Nowy Tomysl
Key facts
| Inspection ID | 305076 |
|---|---|
| Firm | Aesculap-Chifa SP. Z.O.O. |
| FEI number | 3002315844 |
| Address | Ul. Tysiaclecia 14 |
| City | Nowy Tomysl |
| Fiscal year | 2004 |
| Inspection end date | Dec 11, 2003 |
| 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
- 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