FDA Inspection 940792 — Defibtech, LLC
The FDA completed an inspection of Defibtech, LLC on Aug 27, 2015 in Seymour, 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 27, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Seymour, CT (United States)