# Classic Delight LLC, Saint Marys, OH – FDA Inspections

Source: https://www.keypedia.com/companies/classic-delight-llc/832cc55e-ea26-4fb5-871c-592b86d2ae45

> Inspection records and compliance data for Classic Delight LLC in Saint Marys, Ohio. 7 FDA inspections on record, last inspected June 04, 2024.

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## Details

- Name: Classic Delight LLC
- FEI Number: 1000122708
- Address Line 1: 310 S Park Dr
- City: Saint Marys
- State: Ohio
- Zip Code: 45885
- Country Name: United States
- Address: 310 S Park Dr, Saint Marys, Ohio 45885, United States
- Country: United States

## Related Documents

- [FDA Inspection 1240294 - Classic Delight LLC - 2024-06-04](https://www.keypedia.com/records/fda_inspections/classic-delight-llc/9410c904-f80a-4c8c-aa65-109221bf0b72) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 4, 2024
- FDA Inspection 1154499 - Classic Delight LLC - 2021-09-23 — classification: No Action Indicated (NAI), source: FDA, date: September 23, 2021
- FDA Inspection 1063051 - Classic Delight LLC - 2018-08-23 — classification: No Action Indicated (NAI), source: FDA, date: August 23, 2018
- FDA Inspection 1028782 - Classic Delight LLC - 2017-09-01 — classification: No Action Indicated (NAI), source: FDA, date: September 1, 2017
- FDA Inspection 1028782 - Classic Delight LLC - 2017-09-01 — classification: No Action Indicated (NAI), source: FDA, date: September 1, 2017
- FDA Inspection 1028782 - Classic Delight LLC - 2017-09-01 — classification: No Action Indicated (NAI), source: FDA, date: September 1, 2017
- FDA Inspection 926857 - Classic Delight LLC - 2015-05-06 — classification: No Action Indicated (NAI), source: FDA, date: May 6, 2015
- FDA Inspection 926857 - Classic Delight LLC - 2015-05-06 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 6, 2015
- FDA Inspection 926857 - Classic Delight LLC - 2015-05-06 — classification: No Action Indicated (NAI), source: FDA, date: May 6, 2015
- FDA Inspection 708711 - Classic Delight LLC - 2011-02-08 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 8, 2011

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