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FDA Inspection 563269 — Titan Implants, Inc

Titan Implants, Inc — FEI 3003024548

The FDA completed an inspection of Titan Implants, Inc on February 17, 2009 in Bergenfield, NJ. 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
February 17, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Bergenfield, NJ (United States)

Facility

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