FDA inspection
Germaine Laboratories, Inc: FDA inspection ending Mar 14, 2014
FDA inspection 876841 · Voluntary Action Indicated (VAI) · San Antonio, TX
Key facts
| Inspection ID | 876841 |
|---|---|
| Firm | Germaine Laboratories, Inc |
| FEI number | 3001451797 |
| Address | 11030 Wye Dr |
| City | San Antonio |
| State | TX |
| ZIP | 78217-2616 |
| Fiscal year | 2014 |
| Inspection end date | Mar 14, 2014 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Medical 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