FDA Inspection
Vonco Products, Inc.Vonco Products, Inc. – FDA Inspection, Apr 10, 2025
Record Details
This FDA Inspection record concerns Vonco Products, Inc., with an inspection on April 10, 2025, issued by the Minneapolis District Office, covering medical devices & rad health.
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ID · 94904815-8ef8-424b-9c54-6879d39598a2
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1266449
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Medical Devices
FDA Citations
4- 21 CFR 820.75(c)Process changes - review, evaluation and revalidation
- 21 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
- 21 CFR 820.30(c)Design input - Lack of or inadequate procedures
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
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Other FDA inspections of Vonco Products, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| June 29, 2017 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Vonco Products, Inc.
- FDA Inspection 1018591 - 2017-06-29
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