FDA inspection
Lee Products Company: FDA inspection ending Sep 28, 2016
FDA inspection 989124 · No Action Indicated (NAI) · Minneapolis, MN
Key facts
| Inspection ID | 989124 |
|---|---|
| Firm | Lee Products Company |
| FEI number | 2111564 |
| Address | 800 E 80th St |
| City | Minneapolis |
| State | MN |
| ZIP | 55420 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Sep 28, 2016 |
| Classification | No Action Indicated (NAI) |
| Project area | Colors and Cosmetics Technology |
| 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