FDA Inspection 827925 — Philips Electronics North America Corporation
The FDA completed an inspection of Philips Electronics North America Corporation on Apr 17, 2013 in Stamford, CT. 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
- Apr 17, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Stamford, CT (United States)