FDA Inspection 588443 — Confluent Medical Technologies, Inc.
The FDA completed an inspection of Confluent Medical Technologies, Inc. on June 11, 2009 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
- June 11, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Fremont, CA (United States)
Additional Details
Postmarket Audit Inspections