FDA Inspection 777655 — IsoTis OrthoBiologics, Inc.

IsoTis OrthoBiologics, Inc. — FEI 3001503333

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