FDA inspection
Keurig Dr Pepper Inc.: FDA inspection ending Oct 22, 2012
FDA inspection 804261 · No Action Indicated (NAI) · Austin, TX
Key facts
| Inspection ID | 804261 |
|---|---|
| Firm | Keurig Dr Pepper Inc. |
| FEI number | 1622841 |
| Address | 2120 Grand Avenue Pkwy Ste 200 |
| City | Austin |
| State | TX |
| ZIP | 78728 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Oct 22, 2012 |
| Classification | No Action Indicated (NAI) |
| Project area | Foodborne Biological Hazards |
| Product type | Food/Cosmetics |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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