FDA Inspection 838101 — ReShape Lifesciences, Inc.
The FDA completed an inspection of ReShape Lifesciences, Inc. on June 17, 2013 in Eden Prairie, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- June 17, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Eden Prairie, MN (United States)