FDA inspection
ReShape Lifesciences, Inc.: FDA inspection ending Apr 22, 2016
FDA inspection 974242 · No Action Indicated (NAI) · Eden Prairie, MN
Key facts
| Inspection ID | 974242 |
|---|---|
| Firm | ReShape Lifesciences, Inc. |
| FEI number | 3005025697 |
| Address | 2800 Patton Rd |
| City | Eden Prairie |
| State | MN |
| ZIP | 55344 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Apr 22, 2016 |
| Classification | No Action Indicated (NAI) |
| Project area | Project Evaluation: 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