FDA Inspection 823920 — ABB, Inc.
The FDA completed an inspection of ABB, Inc. on Mar 21, 2013 in Auburn Hills, MI. 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
- Mar 21, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Auburn Hills, MI (United States)