# Dixie Dew Products Inc - Inspection Records

Source: https://www.keypedia.com/companies/dixie-dew-products-inc/6eb4ab20-b010-4749-9a8f-74487198321d

> Inspection records and compliance data for Dixie Dew Products Inc in Erlanger, Kentucky. Access full analysis and detailed observations.

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## Details

- Name: Dixie Dew Products Inc
- FEI Number: 1022121
- City: Erlanger
- State: Kentucky
- Country Name: United States
- Address Line 1: 1360 Jamike Ave
- Zip Code: 41018
- Facility Type: Manufacturer

## Related Documents

- [FDA Inspection 1032243 - Dixie Dew Products Inc - 2017-10-26](https://www.keypedia.com/records/fda_inspections/dixie-dew-products-inc/8ddb17d7-4065-46b3-a808-3fac93400675) — classification: Official Action Indicated (OAI), source: FDA, date: October 26, 2017
- [FDA Inspection 1032242 - Dixie Dew Products Inc - 2017-09-26](https://www.keypedia.com/records/fda_inspections/dixie-dew-products-inc/55b93435-2d8c-412c-95df-8da2a8b44930) — classification: Official Action Indicated (OAI), source: FDA, date: September 26, 2017
- [FDA Inspection 1015991 - Dixie Dew Products Inc - 2017-06-28](https://www.keypedia.com/records/fda_inspections/dixie-dew-products-inc/f7ce4f93-f71e-4f35-a3a9-b40f89bc54b4) — classification: Official Action Indicated (OAI), source: FDA, date: June 28, 2017
- [FDA Inspection 1010712 - Dixie Dew Products Inc - 2017-04-13](https://www.keypedia.com/records/fda_inspections/dixie-dew-products-inc/69a80a83-9394-4813-9aa4-8877ea599c88) — classification: Official Action Indicated (OAI), source: FDA, date: April 13, 2017
- [483 - Dixie Dew Products Inc - 2017-03-15](https://www.keypedia.com/records/483/dixie-dew-products-inc/00f39388-80e5-46d5-a562-ec7abe844936) — source: FDA, date: March 15, 2017
- [FDA Inspection 1000596 - Dixie Dew Products Inc - 2017-02-07](https://www.keypedia.com/records/fda_inspections/dixie-dew-products-inc/95ee6030-e66d-4448-a4a5-81185f57fa3a) — classification: No Action Indicated (NAI), source: FDA, date: February 7, 2017
- [FDA Inspection 886681 - Dixie Dew Products Inc - 2014-07-10](https://www.keypedia.com/records/fda_inspections/dixie-dew-products-inc/cb901c40-ca35-45ae-a6ef-267e835a95e5) — classification: No Action Indicated (NAI), source: FDA, date: July 10, 2014
- [FDA Inspection 886681 - Dixie Dew Products Inc - 2014-07-10](https://www.keypedia.com/records/fda_inspections/dixie-dew-products-inc/1031205f-ea92-43b4-ac04-343a9c625d86) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 10, 2014
- [FDA Inspection 731248 - Dixie Dew Products Inc - 2011-06-23](https://www.keypedia.com/records/fda_inspections/dixie-dew-products-inc/38704e14-d2a1-4120-bdb0-b10b40413bc1) — classification: No Action Indicated (NAI), source: FDA, date: June 23, 2011
- [FDA Inspection 666966 - Dixie Dew Products Inc - 2010-06-23](https://www.keypedia.com/records/fda_inspections/dixie-dew-products-inc/4fd7ac6e-e45e-401d-8d86-f7f5e6e33874) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 23, 2010
- [FDA Inspection 666966 - Dixie Dew Products Inc - 2010-06-23](https://www.keypedia.com/records/fda_inspections/dixie-dew-products-inc/9fe2f713-853b-41ec-bbfe-26717f22f105) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 23, 2010

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