FDA Inspection 1249628 — Vanguard EMS, Inc.

Vanguard EMS, Inc. — FEI 3004363082

The FDA completed an inspection of Vanguard EMS, Inc. on September 20, 2024 in Beaverton, OR. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 20, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Beaverton, OR (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
313021 CFR 820.100(a)Lack of or inadequate procedures