FDA inspection
Gyne Tech Instruments Corp: FDA inspection ending Apr 24, 2002
FDA inspection 213202 · No Action Indicated (NAI) · Burbank, CA
Key facts
| Inspection ID | 213202 |
|---|---|
| Firm | Gyne Tech Instruments Corp |
| FEI number | 2020587 |
| Address | 1115 Chestnut St |
| City | Burbank |
| State | CA |
| ZIP | 91506-1624 |
| Fiscal year | 2002 |
| Inspection end date | Apr 24, 2002 |
| 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