FDA inspection
Muji U.S.A. Limited: FDA inspection ending May 16, 2019
FDA inspection 1090239 · Voluntary Action Indicated (VAI) · New York, NY
Key facts
| Inspection ID | 1090239 |
|---|---|
| Firm | Muji U.S.A. Limited |
| FEI number | 3006160107 |
| Address | 250 W 39th St Rm 202 |
| City | New York |
| State | NY |
| ZIP | 10018 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | May 16, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Foodborne Biological Hazards |
| Product type | Food/Cosmetics |
At a glance
- None Citations
- 1–9 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