FDA Inspection 1227305 — Vesper Medical, Inc.
The FDA completed an inspection of Vesper Medical, Inc. on Jan 8, 2024 in Wayne, PA. 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
- Jan 8, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Wayne, PA (United States)
Additional Details
Sponsor, Contract Research Organization