FDA inspection
Miyoshi America, Inc: FDA inspection ending Nov 17, 2015
FDA inspection 950532 · No Action Indicated (NAI) · Dayville, CT
Key facts
| Inspection ID | 950532 |
|---|---|
| Firm | Miyoshi America, Inc |
| FEI number | 3009481791 |
| Address | 110 Louisa Viens Dr |
| City | Dayville |
| State | CT |
| ZIP | 06241 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Nov 17, 2015 |
| 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