FDA Inspection 998392 — VasSol, Inc.
The FDA completed an inspection of VasSol, Inc. on Nov 17, 2016 in River Forest, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Nov 17, 2016
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- River Forest, IL (United States)