FDA Inspection 1107557 — Spatz FGIA, Inc

Spatz FGIA, Inc — FEI 3015409025

The FDA completed an inspection of Spatz FGIA, Inc on September 25, 2019 in Ra'Anana. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 25, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Ra'Anana (Israel)