FDA Inspection 568755 — ARKRAY, Inc.
The FDA completed an inspection of ARKRAY, Inc. on Feb 9, 2009 in Kyoto. 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
- Feb 9, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Kyoto (Japan)