FDA Inspection 1001618 — Phoenix Instruments Inc.
The FDA completed an inspection of Phoenix Instruments Inc. on January 13, 2017 in Lisle, IL. 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 13, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Lisle, IL (United States)