# Garber Ice Cream Company Inc, Winchester, VA – FDA Inspections

Source: https://www.keypedia.com/companies/garber-ice-cream-company-inc/8d18860f-c5cd-4887-8c07-4881dbc5e987

> Inspection records and compliance data for Garber Ice Cream Company Inc in Winchester, Virginia. 5 FDA inspections on record, last inspected September 12, 2022.

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## Details

- Name: Garber Ice Cream Company Inc
- FEI Number: 1117807
- Address Line 1: 360 Front Royal Pike
- City: Winchester
- State: Virginia
- Zip Code: 22602
- Country Name: United States
- Address: 360 Front Royal Pike, Winchester, Virginia 22602, United States
- Country: United States

## Related Documents

- FDA Inspection 1181497 - Garber Ice Cream Company Inc - 2022-09-12 — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2022
- FDA Inspection 1181497 - Garber Ice Cream Company Inc - 2022-09-12 — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2022
- FDA Inspection 1017025 - Garber Ice Cream Company Inc - 2017-05-15 — classification: No Action Indicated (NAI), source: FDA, date: May 15, 2017
- FDA Inspection 1017025 - Garber Ice Cream Company Inc - 2017-05-15 — classification: No Action Indicated (NAI), source: FDA, date: May 15, 2017
- FDA Inspection 723877 - Garber Ice Cream Company Inc - 2011-05-06 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 6, 2011
- FDA Inspection 723877 - Garber Ice Cream Company Inc - 2011-05-06 — classification: No Action Indicated (NAI), source: FDA, date: May 6, 2011
- FDA Inspection 675846 - Garber Ice Cream Company Inc - 2010-08-03 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 3, 2010
- [FDA Inspection 675846 - Garber Ice Cream Company Inc - 2010-08-03](https://www.keypedia.com/records/fda_inspections/garber-ice-cream-company-inc/891a5ff6-e271-4d38-b00e-152c7b6a7400) — classification: No Action Indicated (NAI), source: FDA, date: August 3, 2010
- FDA Inspection 598625 - Garber Ice Cream Company Inc - 2009-06-30 — classification: No Action Indicated (NAI), source: FDA, date: June 30, 2009

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