FDA inspection
ReShape Lifesciences, Inc.: FDA inspection ending Jun 17, 2013
FDA inspection 838101 · No Action Indicated (NAI) · Eden Prairie, MN
Key facts
| Inspection ID | 838101 |
|---|---|
| Firm | ReShape Lifesciences, Inc. |
| FEI number | 3005025697 |
| Address | 2800 Patton Rd |
| City | Eden Prairie |
| State | MN |
| ZIP | 55344 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Jun 17, 2013 |
| 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