FDA Inspection 562050 — Omron (Dalian) Co., Ltd. (Plant 1)
The FDA completed an inspection of Omron (Dalian) Co., Ltd. (Plant 1) on January 21, 2009 in Dalian. 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
- January 21, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Dalian (China)