FDA inspection
ASAHI POLYSLIDER COMPANY, LIMITED Okayama-Kuse Plant: FDA inspection ending Mar 18, 2004
FDA inspection 321887 · Voluntary Action Indicated (VAI) · Maniwa
Key facts
| Inspection ID | 321887 |
|---|---|
| Firm | ASAHI POLYSLIDER COMPANY, LIMITED Okayama-Kuse Plant |
| FEI number | 1000600761 |
| Address | 860-2 Misaki, Misaki |
| City | Maniwa |
| Fiscal year | 2004 |
| Inspection end date | Mar 18, 2004 |
| 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