FDA Inspection 892451 — Hillcrest Medical Center-Irb

Hillcrest Medical Center-Irb — FEI 1643400

The FDA completed an inspection of Hillcrest Medical Center-Irb on Aug 11, 2014 in Tulsa, OK. 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
Aug 11, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Tulsa, OK (United States)

Additional Details

IRB

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