FDA Inspection 733500 — Titan Implants, Inc

Titan Implants, Inc — FEI 3003024548

The FDA completed an inspection of Titan Implants, Inc on July 6, 2011 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
July 6, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Bergenfield, NJ (United States)