FDA Inspection 1024231 — Defibtech, LLC
The FDA completed an inspection of Defibtech, LLC on Aug 16, 2017 in Branford, 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
- Aug 16, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Branford, CT (United States)