FDA Inspection 1245727 — Van Duzen, Inc.

Van Duzen, Inc. — FEI 3009196021

The FDA completed an inspection of Van Duzen, Inc. on August 2, 2024 in Dallas, TX. 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
August 2, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Dallas, TX (United States)

Citations

IDCFRDescription
54621 CFR 820.75(a)Lack of or inadequate process validation