FDA Inspection 1107557 — Spatz FGIA, Inc

Spatz FGIA, Inc — FEI 3015409025

The FDA completed an inspection of Spatz FGIA, Inc on Sep 25, 2019 in Ra'Anana. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection details

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.