FDA inspection
Multisource Manufacturing, LLC.: FDA inspection ending Dec 17, 2021
FDA inspection 1160326 · Voluntary Action Indicated (VAI) · Fridley, MN
Key facts
| Inspection ID | 1160326 |
|---|---|
| Firm | Multisource Manufacturing, LLC. |
| FEI number | 3011604145 |
| Address | 7500 Commerce Ln Ne |
| City | Fridley |
| State | MN |
| ZIP | 55432 |
| Country | United States |
| Fiscal year | 2022 |
| Inspection end date | Dec 17, 2021 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
At a glance
- 1–9 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