FDA inspection
Xymogen Manufacturing: FDA inspection ending May 24, 2013
FDA inspection 833513 · Official Action Indicated (OAI) · Orlando, FL
Key facts
| Inspection ID | 833513 |
|---|---|
| Firm | Xymogen Manufacturing |
| FEI number | 3004315824 |
| Address | 6900 Kingspointe Pkwy |
| City | Orlando |
| State | FL |
| ZIP | 32819 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | May 24, 2013 |
| Classification | Official Action Indicated (OAI) |
| Project area | Food Composition, Standards, Labeling and Econ |
| Product type | Food/Cosmetics |
At a glance
- 10–99 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