FDA Inspection 1166785 — ProxySoft Worldwide, Inc.
The FDA completed an inspection of ProxySoft Worldwide, Inc. on Apr 6, 2022 in Bethel, CT. 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
- Apr 6, 2022
- Fiscal Year
- 2022
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Bethel, CT (United States)