# Buchanan Hollow Nut Company, Le Grand, CA – FDA Inspections

Source: https://www.keypedia.com/companies/buchanan-hollow-nut-company/5e9fb42f-03fa-4fc9-8481-5c78b35f0cb2

> Inspection records and compliance data for Buchanan Hollow Nut Company in Le Grand, California. 3 FDA inspections on record, last inspected January 07, 2014.

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## Details

- Name: Buchanan Hollow Nut Company
- FEI Number: 2937628
- Address Line 1: 6510 Minturn Rd
- City: Le Grand
- State: California
- Zip Code: 95333
- Country Name: United States
- Address: 6510 Minturn Rd, Le Grand, California 95333, United States
- Country: United States

## Related Documents

- FDA Inspection 862159 - Buchanan Hollow Nut Company - 2014-01-07 — classification: No Action Indicated (NAI), source: FDA, date: January 7, 2014
- FDA Inspection 862159 - Buchanan Hollow Nut Company - 2014-01-07 — classification: No Action Indicated (NAI), source: FDA, date: January 7, 2014
- FDA Inspection 862159 - Buchanan Hollow Nut Company - 2014-01-07 — classification: No Action Indicated (NAI), source: FDA, date: January 7, 2014
- FDA Inspection 862159 - Buchanan Hollow Nut Company - 2014-01-07 — classification: No Action Indicated (NAI), source: FDA, date: January 7, 2014
- FDA Inspection 699525 - Buchanan Hollow Nut Company - 2010-11-12 — classification: No Action Indicated (NAI), source: FDA, date: November 12, 2010
- FDA Inspection 699525 - Buchanan Hollow Nut Company - 2010-11-12 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 12, 2010
- FDA Inspection 699525 - Buchanan Hollow Nut Company - 2010-11-12 — classification: No Action Indicated (NAI), source: FDA, date: November 12, 2010
- FDA Inspection 696971 - Buchanan Hollow Nut Company - 2010-11-12 — classification: No Action Indicated (NAI), source: FDA, date: November 12, 2010
- FDA Inspection 696971 - Buchanan Hollow Nut Company - 2010-11-12 — classification: No Action Indicated (NAI), source: FDA, date: November 12, 2010
- FDA Inspection 696971 - Buchanan Hollow Nut Company - 2010-11-12 — classification: No Action Indicated (NAI), source: FDA, date: November 12, 2010

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