FDA inspection
Needle Specialty Products Corporation: FDA inspection ending Apr 11, 2002
FDA inspection 212912 · Voluntary Action Indicated (VAI) · Boyle, MS
Key facts
| Inspection ID | 212912 |
|---|---|
| Firm | Needle Specialty Products Corporation |
| FEI number | 1000112137 |
| Address | 600 Highway 446 |
| City | Boyle |
| State | MS |
| ZIP | 38730-9673 |
| Fiscal year | 2002 |
| Inspection end date | Apr 11, 2002 |
| 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