# Fioravanti Custom Products - Inspection Records

Source: https://www.globalkeysolutions.net/companies/fioravanti-custom-products/af05c06e-8aa4-4118-964d-9fb542e52813

> Inspection records and compliance data for Fioravanti Custom Products in Portland, Oregon. Access full analysis and detailed observations.

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## Details

- Name: Fioravanti Custom Products
- FEI Number: 3003887109
- City: Portland
- State: Oregon
- Country Name: United States
- Address Line 1: 2211 Nw Nicolai St
- Zip Code: 97210

## Related Documents

- [FDA Inspection 925245 - Fioravanti Custom Products - 2015-03-30](https://www.globalkeysolutions.net/records/fda_inspections/fioravanti-custom-products/35ed5f5d-71a1-4a39-bdff-10afd7ee00f7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 30, 2015
- [FDA Inspection 925245 - Fioravanti Custom Products - 2015-03-30](https://www.globalkeysolutions.net/records/fda_inspections/fioravanti-custom-products/fcd950f9-b9a4-4db1-b0b7-d8cf549eb670) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 30, 2015
- [FDA Inspection 925245 - Fioravanti Custom Products - 2015-03-30](https://www.globalkeysolutions.net/records/fda_inspections/fioravanti-custom-products/95d88bb0-0118-4e73-b010-01e1e80b0f0c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 30, 2015
- [WARNING_LETTER - Fioravanti Custom Products - 2014-04-24](https://www.globalkeysolutions.net/records/warning_letter/fioravanti-custom-products/001795ba-b248-4e90-9416-b5204b12a29f) — source: FDA, date: April 24, 2014
- [FDA Inspection 877616 - Fioravanti Custom Products - 2014-04-24](https://www.globalkeysolutions.net/records/fda_inspections/fioravanti-custom-products/ac86ada8-add6-4ca8-936f-878845ae4fd6) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 24, 2014
- [FDA Inspection 877616 - Fioravanti Custom Products - 2014-04-24](https://www.globalkeysolutions.net/records/fda_inspections/fioravanti-custom-products/ec125a65-dd99-4f23-a319-cf015a1c587b) — classification: Official Action Indicated (OAI), source: FDA, date: April 24, 2014

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## Related Officers

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