FDA Inspection 675878 — Defibtech, LLC
The FDA completed an inspection of Defibtech, LLC on August 18, 2010 in Guilford, CT. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- August 18, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Guilford, CT (United States)