FDA Inspection 1252737 — Viant AS&O Holdings, LLC

Viant AS&O Holdings, LLC — FEI 1218882

The FDA completed an inspection of Viant AS&O Holdings, LLC on Oct 28, 2024 in Brimfield, MA. 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). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 28, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Brimfield, MA (United States)

Citations

IDCFRDescription
312121 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures

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