FDA inspection
ASAHI POLYSLIDER COMPANY, LIMITED Okayama-Kuse Plant: FDA inspection ending Apr 11, 2007
FDA inspection 468031 · No Action Indicated (NAI) · Maniwa
Key facts
| Inspection ID | 468031 |
|---|---|
| Firm | ASAHI POLYSLIDER COMPANY, LIMITED Okayama-Kuse Plant |
| FEI number | 1000600761 |
| Address | 860-2 Misaki, Misaki |
| City | Maniwa |
| Fiscal year | 2007 |
| Inspection end date | Apr 11, 2007 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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