FDA Inspection 876495 — Defibtech, LLC
The FDA completed an inspection of Defibtech, LLC on April 25, 2014 in Guilford, CT. 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
- April 25, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Guilford, CT (United States)