FDA Inspection 1024251 — Confluent Medical Technologies, Inc.
The FDA completed an inspection of Confluent Medical Technologies, Inc. on August 15, 2017 in Fremont, CA. 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
- August 15, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Fremont, CA (United States)