FDA inspection
Unique Global Product and Distribution Inc.: FDA inspection ending Apr 11, 2015
FDA inspection 931035 · No Action Indicated (NAI) · Cambridge
Key facts
| Inspection ID | 931035 |
|---|---|
| Firm | Unique Global Product and Distribution Inc. |
| FEI number | 3011296497 |
| Address | 539 Collier Macmillan Drive, Unit C |
| City | Cambridge |
| Country | Canada |
| Fiscal year | 2015 |
| Inspection end date | Apr 11, 2015 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
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