FDA Inspection 1037675 — Titan Implants, Inc

Titan Implants, Inc — FEI 3003024548

The FDA completed an inspection of Titan Implants, Inc on January 16, 2018 in Bergenfield, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 16, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Bergenfield, NJ (United States)

Citations

IDCFRDescription
407021 CFR 820.30(g)Design validation - documentation