# The Sugarman Of Vermont LLC - Inspection Records

Source: https://www.keypedia.com/companies/the-sugarman-of-vermont-llc/1850a0e3-f0f2-4945-a722-202ac6264d82

> Inspection records and compliance data for The Sugarman Of Vermont LLC in Hardwick, Vermont. Access full analysis and detailed observations.

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## Details

- Name: The Sugarman Of Vermont LLC
- FEI Number: 1000585359
- City: Hardwick
- State: Vermont
- Country Name: United States
- Address Line 1: 84 Industrial Park Road
- Zip Code: 05843

## Related Documents

- [FDA Inspection 1263614 - The Sugarman Of Vermont LLC - 2025-02-03](https://www.keypedia.com/records/fda_inspections/the-sugarman-of-vermont-llc/88e83da6-8918-457f-bc4b-363624966243) — source: FDA, date: February 3, 2025
- [FDA Inspection 1263614 - The Sugarman Of Vermont LLC - 2025-02-03](https://www.keypedia.com/records/fda_inspections/the-sugarman-of-vermont-llc/5009b892-e363-409c-be82-21a83d0d4fdd) — classification: No Action Indicated (NAI), source: FDA, date: February 3, 2025
- [FDA Inspection 1167053 - The Sugarman Of Vermont LLC - 2022-04-06](https://www.keypedia.com/records/fda_inspections/the-sugarman-of-vermont-llc/a223845f-e51e-4033-ace4-ac2899b8ed13) — classification: No Action Indicated (NAI), source: FDA, date: April 6, 2022
- [FDA Inspection 1039003 - The Sugarman Of Vermont LLC - 2018-01-30](https://www.keypedia.com/records/fda_inspections/the-sugarman-of-vermont-llc/916067a7-4f7d-45b6-a665-9e510b501cc0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 30, 2018
- [FDA Inspection 933205 - The Sugarman Of Vermont LLC - 2015-05-20](https://www.keypedia.com/records/fda_inspections/the-sugarman-of-vermont-llc/ea92caad-e3e9-4302-adc9-3ee3855db198) — classification: No Action Indicated (NAI), source: FDA, date: May 20, 2015
- [FDA Inspection 780538 - The Sugarman Of Vermont LLC - 2012-04-25](https://www.keypedia.com/records/fda_inspections/the-sugarman-of-vermont-llc/b31657ad-9e27-46a7-973f-8bf8f4f29ae0) — classification: No Action Indicated (NAI), source: FDA, date: April 25, 2012

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