FDA Inspection 588443 — Confluent Medical Technologies, Inc.

Confluent Medical Technologies, Inc. — FEI 3007635982

The FDA completed an inspection of Confluent Medical Technologies, Inc. on Jun 11, 2009 in Fremont, CA. 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
Jun 11, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Fremont, CA (United States)

Additional details

Postmarket Audit Inspections

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