FDA Inspection 777655 — IsoTis OrthoBiologics, Inc.

IsoTis OrthoBiologics, Inc. — FEI 3001503333

The FDA completed an inspection of IsoTis OrthoBiologics, Inc. on Apr 27, 2012 in Irvine, 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
Apr 27, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Irvine, CA (United States)

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