FDA inspection
Contrapak: FDA inspection ending Apr 17, 2000
FDA inspection 20082 · No Action Indicated (NAI) · Dallas, TX
Key facts
| Inspection ID | 20082 |
|---|---|
| Firm | Contrapak |
| FEI number | 3002988839 |
| Address | 4925 Greenville Ave Ste 225 |
| City | Dallas |
| State | TX |
| ZIP | 75206-4088 |
| Fiscal year | 2000 |
| Inspection end date | Apr 17, 2000 |
| Classification | No Action Indicated (NAI) |
| Project area | Tech Assist: Food & Cosmetics |
| 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