FDA Inspection 1334316 — Veritiv Operating Company

Veritiv Operating Company — FEI 3018326554

The FDA completed an inspection of Veritiv Operating Company on Sep 4, 2026 in Grapevine, TX. 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). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 4, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Grapevine, TX (United States)

Citations

IDCFRDescription
23075ISO 13485:2016 Clause 6.2(e)Records of personnel competence not maintained
23200ISO 13485:2016 Clause 7.6Equipment calibration or verification not performed
23239ISO 13485:2016 Clause 8.3.1Records of nonconforming product and actions taken not maintained

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