FDA inspection
Xymogen Manufacturing: FDA inspection ending Aug 1, 2011
FDA inspection 737870 · Official Action Indicated (OAI) · Orlando, FL
Key facts
| Inspection ID | 737870 |
|---|---|
| Firm | Xymogen Manufacturing |
| FEI number | 3004315824 |
| Address | 6900 Kingspointe Pkwy |
| City | Orlando |
| State | FL |
| ZIP | 32819 |
| Country | United States |
| Fiscal year | 2011 |
| Inspection end date | Aug 1, 2011 |
| Classification | Official Action Indicated (OAI) |
| Project area | Colors and Cosmetics Technology |
| Product type | Food/Cosmetics |
At a glance
- 1–9 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