# Riverfront Egg Robbers Inc., Biscoe, AR – FDA Inspections

Source: https://www.keypedia.com/companies/riverfront-egg-robbers-inc/ff6b3bd3-5c44-4698-a8c3-35bd4f56a37d

> Inspection records and compliance data for Riverfront Egg Robbers Inc. in Biscoe, Arkansas. 6 FDA inspections on record (1 OAI), 1 warning letter, last inspected February 07, 2017.

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## Details

- Name: Riverfront Egg Robbers Inc.
- FEI Number: 3003589093
- Address Line 1: 13757 Highway 70 East
- City: Biscoe
- State: Arkansas
- Zip Code: 72017
- Country Name: United States
- Address: 13757 Highway 70 East, Biscoe, Arkansas 72017, United States
- Country: United States

## Related Documents

- FDA Inspection 1001717 - Riverfront Egg Robbers Inc. - 2017-02-07 — classification: No Action Indicated (NAI), source: FDA, date: February 7, 2017
- FDA Inspection 871923 - Riverfront Egg Robbers Inc. - 2014-02-19 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 19, 2014
- FDA Inspection 813341 - Riverfront Egg Robbers Inc. - 2012-12-18 — classification: No Action Indicated (NAI), source: FDA, date: December 18, 2012
- [WARNING_LETTER - Riverfront Egg Robbers Inc. - 2012-01-12](https://www.keypedia.com/records/warning_letter/riverfront-egg-robbers-inc/b3d9402b-59e5-49fd-937c-9f370ca8d954) — source: FDA, date: January 12, 2012
- [FDA Inspection 763992 - Riverfront Egg Robbers Inc. - 2012-01-12](https://www.keypedia.com/records/fda_inspections/riverfront-egg-robbers-inc/16bf6579-2079-4878-a31e-5c1f8a103adb) — classification: Official Action Indicated (OAI), source: FDA, date: January 12, 2012
- [FDA Inspection 643576 - Riverfront Egg Robbers Inc. - 2010-01-27](https://www.keypedia.com/records/fda_inspections/riverfront-egg-robbers-inc/21378d39-d363-427e-b5bb-0cb4ee5b2b5e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 27, 2010
- [FDA Inspection 575384 - Riverfront Egg Robbers Inc. - 2009-03-25](https://www.keypedia.com/records/fda_inspections/riverfront-egg-robbers-inc/dc580420-acf6-415f-bba9-3e6971f6a01b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 25, 2009

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