FDA inspection
Germaine Laboratories, Inc: FDA inspection ending Mar 11, 2010
FDA inspection 660026 · No Action Indicated (NAI) · San Antonio, TX
Key facts
| Inspection ID | 660026 |
|---|---|
| Firm | Germaine Laboratories, Inc |
| FEI number | 3001451797 |
| Address | 11030 Wye Dr |
| City | San Antonio |
| State | TX |
| ZIP | 78217-2616 |
| Fiscal year | 2010 |
| Inspection end date | Mar 11, 2010 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Medical 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