# Vermont Creamery, LLC, Websterville, VT – FDA Inspections

Source: https://www.keypedia.com/companies/vermont-creamery-llc/e207ebb1-4ab9-48e4-ad8e-5008847c4e75

> Inspection records and compliance data for Vermont Creamery, LLC in Websterville, Vermont. 8 FDA inspections on record, last inspected August 24, 2026.

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## Details

- Name: Vermont Creamery, LLC
- FEI Number: 1000120589
- Address Line 1: 40 Pitman Road
- City: Websterville
- State: Vermont
- Zip Code: 05678
- Country Name: United States
- Address: 40 Pitman Road, Websterville, Vermont 05678, United States
- Country: United States

## Related Documents

- FDA Inspection 1334160 - Vermont Creamery, LLC - 2026-08-24 — classification: No Action Indicated (NAI), source: FDA, date: August 24, 2026
- FDA Inspection 1286166 - Vermont Creamery, LLC - 2025-10-30 — source: FDA, date: October 30, 2025
- FDA Inspection 1286166 - Vermont Creamery, LLC - 2025-10-30 — classification: No Action Indicated (NAI), source: FDA, date: October 30, 2025
- FDA Inspection 1209769 - Vermont Creamery, LLC - 2023-06-29 — classification: No Action Indicated (NAI), source: FDA, date: June 29, 2023
- FDA Inspection 1209769 - Vermont Creamery, LLC - 2023-06-29 — classification: No Action Indicated (NAI), source: FDA, date: June 29, 2023
- FDA Inspection 1071585 - Vermont Creamery, LLC - 2018-10-30 — classification: No Action Indicated (NAI), source: FDA, date: October 30, 2018
- FDA Inspection 972471 - Vermont Creamery, LLC - 2016-04-21 — classification: No Action Indicated (NAI), source: FDA, date: April 21, 2016
- FDA Inspection 816291 - Vermont Creamery, LLC - 2013-01-30 — classification: No Action Indicated (NAI), source: FDA, date: January 30, 2013
- [FDA Inspection 677007 - Vermont Creamery, LLC - 2010-08-18](https://www.keypedia.com/records/fda_inspections/vermont-creamery-llc/0709d71c-47a8-458e-a554-ad322c5309be) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 18, 2010
- FDA Inspection 594696 - Vermont Creamery, LLC - 2009-06-17 — classification: No Action Indicated (NAI), source: FDA, date: June 17, 2009

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