# Vonco Products, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/vonco-products-inc/fb16833e-b4b9-4d06-81d0-b597853d548e

> Inspection records and compliance data for Vonco Products, Inc. in Trevor, Wisconsin. Access full analysis and detailed observations.

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## Details

- Name: Vonco Products, Inc.
- FEI Number: 1419562
- City: Trevor
- State: Wisconsin
- Country Name: United States
- Address Line 1: 10826 250th Ave
- Zip Code: 53179

## Related Documents

- [483 - Vonco Products, Inc. - 2025-04-10](https://www.keypedia.com/records/483/vonco-products-inc/9098da6a-4621-4c78-afd0-9e36cafbea41) — source: FDA, date: April 10, 2025
- [FDA Inspection 1266449 - Vonco Products, Inc. - 2025-04-10](https://www.keypedia.com/records/fda_inspections/vonco-products-inc/53010dad-273d-4566-a60f-20701cb99cc1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 10, 2025
- [FDA Inspection 1266449 - Vonco Products, Inc. - 2025-04-10](https://www.keypedia.com/records/fda_inspections/vonco-products-inc/94904815-8ef8-424b-9c54-6879d39598a2) — classification: No Action Indicated (NAI), source: FDA, date: April 10, 2025
- [FDA Inspection 1266449 - Vonco Products, Inc. - 2025-04-10](https://www.keypedia.com/records/fda_inspections/vonco-products-inc/fe29af38-a1e8-44b1-8159-fcf3bca88f7c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 10, 2025
- [FDA Inspection 1266449 - Vonco Products, Inc. - 2025-04-10](https://www.keypedia.com/records/fda_inspections/vonco-products-inc/d92f199a-043f-4c1f-ad65-30aee8ff2c1b) — classification: No Action Indicated (NAI), source: FDA, date: April 10, 2025
- [FDA Inspection 1018591 - Vonco Products, Inc. - 2017-06-29](https://www.keypedia.com/records/fda_inspections/vonco-products-inc/49b4e988-c3ab-455d-a6e5-dbf93e457bf3) — classification: No Action Indicated (NAI), source: FDA, date: June 29, 2017
- [FDA Inspection 1018591 - Vonco Products, Inc. - 2017-06-29](https://www.keypedia.com/records/fda_inspections/vonco-products-inc/ac2af526-69a4-4ed0-b0c4-9ff16dc4f7bb) — classification: No Action Indicated (NAI), source: FDA, date: June 29, 2017

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