FDA inspection
Re-Vita Manufacturing Co., Inc.: FDA inspection ending Mar 8, 2016
FDA inspection 983151 · Orange Park, FL
Key facts
| Inspection ID | 983151 |
|---|---|
| Firm | Re-Vita Manufacturing Co., Inc. |
| FEI number | 1000113282 |
| Address | 153 Industrial Loop S |
| City | Orange Park |
| State | FL |
| ZIP | 32073-6259 |
| Fiscal year | 2016 |
| Inspection end date | Mar 8, 2016 |
| Product type | Food/Cosmetics |
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