FDA inspection
Multisource Manufacturing LLC: FDA inspection ending Feb 9, 2017
FDA inspection 1001755 · No Action Indicated (NAI) · Ramsey, MN
Key facts
| Inspection ID | 1001755 |
|---|---|
| Firm | Multisource Manufacturing LLC |
| FEI number | 3004181214 |
| Address | 6690 Sunwood Dr NW |
| City | Ramsey |
| State | MN |
| ZIP | 55303 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Feb 9, 2017 |
| 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