FDA inspection
Exxonmobil Product Solutions Company: FDA inspection ending Dec 11, 2019
FDA inspection 1116384 · No Action Indicated (NAI) · Baton Rouge, LA
Key facts
| Inspection ID | 1116384 |
|---|---|
| Firm | Exxonmobil Product Solutions Company |
| FEI number | 2313361 |
| Address | 4999 Scenic Hwy |
| City | Baton Rouge |
| State | LA |
| ZIP | 70805 |
| Country | United States |
| Fiscal year | 2020 |
| Inspection end date | Dec 11, 2019 |
| Classification | No Action Indicated (NAI) |
| Project area | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| Product type | Veterinary |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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