FDA Inspection
Veritiv Operating CompanyVeritiv Operating Company – FDA Inspection, Sep 4, 2026
Record Details
This FDA Inspection record concerns Veritiv Operating Company, with an inspection on September 4, 2026, issued by the Center for Devices and Radiological Health, covering medical devices & rad health.
- Company
- Veritiv Operating Company
- Inspection Date
- September 4, 2026
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 78923cdf-fc8d-46a5-94aa-e71ccba0d01c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1334316
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
6- ISO 13485:2016 Clause 4.1.6Equipment calibration or verification not performed
- ISO 13485:2016 Clause 6.2(a)Records of personnel competence not maintained
- ISO 13485:2016 Clause 8.5.1Records of nonconforming product and actions taken not maintained
- ISO 13485:2016 Clause 6.2(e)Records of personnel competence not maintained
- ISO 13485:2016 Clause 7.6Equipment calibration or verification not performed
- ISO 13485:2016 Clause 8.3.1Records of nonconforming product and actions taken not maintained
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Veritiv Operating Company
1| Date | Classification | Office | Project area |
|---|---|---|---|
| January 23, 2024 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Veritiv Operating Company
- FDA Inspection 1230376 - 2024-01-23
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