FDA inspection
LISI MEDICAL Remmele, Inc: FDA inspection ending Jul 14, 2005
FDA inspection 386170 · No Action Indicated (NAI) · Coon Rapids, MN
Key facts
| Inspection ID | 386170 |
|---|---|
| Firm | LISI MEDICAL Remmele, Inc |
| FEI number | 3000203391 |
| Address | 441 93rd Ave Nw |
| City | Coon Rapids |
| State | MN |
| ZIP | 55433-5803 |
| Fiscal year | 2005 |
| Inspection end date | Jul 14, 2005 |
| Classification | No Action Indicated (NAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes 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