FDA Inspection 618535 — Caliber Imaging and Diagnostics, Inc.
The FDA completed an inspection of Caliber Imaging and Diagnostics, Inc. on August 7, 2009 in Rochester, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- August 7, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Rochester, NY (United States)