# Rabbit Creek Products Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/rabbit-creek-products-inc/58d1c281-5666-4bc8-8ecd-1b9f5ab80341

> Inspection records and compliance data for Rabbit Creek Products Inc. in Louisburg, Kansas. Access full analysis and detailed observations.

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## Details

- Name: Rabbit Creek Products Inc.
- FEI Number: 1930153
- City: Louisburg
- State: Kansas
- Country Name: United States
- Address Line 1: 903 N Broadway St
- Zip Code: 66053

## Related Documents

- [FDA Inspection 1064630 - Rabbit Creek Products Inc. - 2018-07-25](https://www.globalkeysolutions.net/records/fda_inspections/rabbit-creek-products-inc/508b058d-123d-494b-861d-af6ec0c0b979) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 25, 2018
- [FDA Inspection 990492 - Rabbit Creek Products Inc. - 2016-10-12](https://www.globalkeysolutions.net/records/fda_inspections/rabbit-creek-products-inc/3b6d5bec-0811-41ef-97bd-2bbedf32513b) — classification: No Action Indicated (NAI), source: FDA, date: October 12, 2016
- [FDA Inspection 830896 - Rabbit Creek Products Inc. - 2013-05-06](https://www.globalkeysolutions.net/records/fda_inspections/rabbit-creek-products-inc/46d17cbe-fca0-4b1e-a956-702a37e365b9) — classification: No Action Indicated (NAI), source: FDA, date: May 6, 2013
- [FDA Inspection 830896 - Rabbit Creek Products Inc. - 2013-05-06](https://www.globalkeysolutions.net/records/fda_inspections/rabbit-creek-products-inc/9a5048dc-0997-4a72-af18-9a5652cf6b5b) — classification: No Action Indicated (NAI), source: FDA, date: May 6, 2013
- [FDA Inspection 764736 - Rabbit Creek Products Inc. - 2012-01-24](https://www.globalkeysolutions.net/records/fda_inspections/rabbit-creek-products-inc/b2d90f62-24a2-4585-97ba-33f9b9551445) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 24, 2012
- [FDA Inspection 764736 - Rabbit Creek Products Inc. - 2012-01-24](https://www.globalkeysolutions.net/records/fda_inspections/rabbit-creek-products-inc/67eaecd8-6187-43a4-b635-4160216fd88d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 24, 2012

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