FDA inspection
Mullinix Packages Inc: FDA inspection ending Oct 14, 1999
FDA inspection 709 · No Action Indicated (NAI) · Fort Wayne, IN
Key facts
| Inspection ID | 709 |
|---|---|
| Firm | Mullinix Packages Inc |
| FEI number | 3001624104 |
| Address | 3511 Engle Rd |
| City | Fort Wayne |
| State | IN |
| ZIP | 46809-1117 |
| Fiscal year | 2000 |
| Inspection end date | Oct 14, 1999 |
| Classification | No Action Indicated (NAI) |
| Project area | Foodborne Biological Hazard |
| 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