# Furst-McNess Company - Inspection Records

Source: https://www.keypedia.com/companies/furst-mcness-company/a0e0b41f-757f-41c6-9086-65ce84697e2a

> Inspection records and compliance data for Furst-McNess Company in Lake City, Florida. Access full analysis and detailed observations.

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## Details

- Name: Furst-McNess Company
- FEI Number: 3002787852
- City: Lake City
- State: Florida
- Country Name: United States
- Address Line 1: 668 Nw Waldo St
- Zip Code: 32055

## Related Documents

- [FDA Inspection 1269959 - Furst-McNess Company - 2025-04-29](https://www.keypedia.com/records/fda_inspections/furst-mcness-company/b22273c0-2d0d-4d56-b90e-3d79a2c97dd7) — source: FDA, date: April 29, 2025
- [FDA Inspection 1269959 - Furst-McNess Company - 2025-04-29](https://www.keypedia.com/records/fda_inspections/furst-mcness-company/14d7b4b4-df54-40be-a204-090a54c0aaa0) — classification: No Action Indicated (NAI), source: FDA, date: April 29, 2025
- [483 - Furst-McNess Company - 2024-05-31](https://www.keypedia.com/records/483/furst-mcness-company/d985cc43-759b-43cc-90e2-ee8469cc6975) — source: FDA, date: May 31, 2024
- [FDA Inspection 1239909 - Furst-McNess Company - 2024-05-31](https://www.keypedia.com/records/fda_inspections/furst-mcness-company/73110de8-bf22-4963-b211-a1970c8fa0ce) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 31, 2024
- [FDA Inspection 1103480 - Furst-McNess Company - 2019-09-17](https://www.keypedia.com/records/fda_inspections/furst-mcness-company/8b6bd145-3dfb-4a86-803e-09049d6c39a7) — classification: No Action Indicated (NAI), source: FDA, date: September 17, 2019
- [FDA Inspection 939358 - Furst-McNess Company - 2015-08-24](https://www.keypedia.com/records/fda_inspections/furst-mcness-company/15b4fba9-7457-46c2-8145-8bbed0e98ba1) — classification: No Action Indicated (NAI), source: FDA, date: August 24, 2015
- [FDA Inspection 570622 - Furst-McNess Company - 2009-03-12](https://www.keypedia.com/records/fda_inspections/furst-mcness-company/a2a856bd-dfb5-48b6-814c-8123ffeaa589) — classification: No Action Indicated (NAI), source: FDA, date: March 12, 2009

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