# Chapel's Country Creamery, LLC, Easton, MD – FDA Inspections

Source: https://www.keypedia.com/companies/chapels-country-creamery-llc/2ebbadbd-b3b5-409d-9e41-381d5bc3e439

> Inspection records and compliance data for Chapel's Country Creamery, LLC in Easton, Maryland. 6 FDA inspections on record, last inspected July 06, 2022.

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## Details

- Name: Chapel's Country Creamery, LLC
- FEI Number: 3008002196
- Address Line 1: 10380 Chapel Rd
- City: Easton
- State: Maryland
- Zip Code: 21601
- Country Name: United States
- Address: 10380 Chapel Rd, Easton, Maryland 21601, United States
- Country: United States

## Related Documents

- FDA Inspection 1179130 - Chapel's Country Creamery, LLC - 2022-07-06 — classification: No Action Indicated (NAI), source: FDA, date: July 6, 2022
- FDA Inspection 1179130 - Chapel's Country Creamery, LLC - 2022-07-06 — classification: No Action Indicated (NAI), source: FDA, date: July 6, 2022
- FDA Inspection 1070342 - Chapel's Country Creamery, LLC - 2018-09-12 — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2018
- FDA Inspection 881418 - Chapel's Country Creamery, LLC - 2014-05-14 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 14, 2014
- FDA Inspection 881418 - Chapel's Country Creamery, LLC - 2014-05-14 — classification: No Action Indicated (NAI), source: FDA, date: May 14, 2014
- FDA Inspection 742125 - Chapel's Country Creamery, LLC - 2011-08-30 — classification: No Action Indicated (NAI), source: FDA, date: August 30, 2011
- [FDA Inspection 742441 - Chapel's Country Creamery, LLC - 2011-08-22](https://www.keypedia.com/records/fda_inspections/chapels-country-creamery-llc/71f1cb2f-ab05-4cd4-9a8a-d6a9998af9b9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 22, 2011
- [FDA Inspection 667925 - Chapel's Country Creamery, LLC - 2010-06-21](https://www.keypedia.com/records/fda_inspections/chapels-country-creamery-llc/eee88251-9440-4def-9fc8-584499b5265b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 21, 2010

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