FDA inspection
Greatbatch Medical: FDA inspection ending May 25, 2016
FDA inspection 974240 · No Action Indicated (NAI) · Plymouth, MN
Key facts
| Inspection ID | 974240 |
|---|---|
| Firm | Greatbatch Medical |
| FEI number | 2183787 |
| Address | 2300 Berkshire Ln N |
| City | Plymouth |
| State | MN |
| ZIP | 55441 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | May 25, 2016 |
| Classification | No Action Indicated (NAI) |
| Project area | Project Evaluation: 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
- 10–99 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