# Raca Enterprises, Inc. dba Life Cycle Herbal Products - Inspection Records

Source: https://www.keypedia.com/companies/raca-enterprises-inc-dba-life-cycle-herbal-products/46ec227b-8b0b-4cd4-862e-c05500c5830c

> Inspection records and compliance data for Raca Enterprises, Inc. dba Life Cycle Herbal Products in El Monte, California. Access full analysis and detailed observations.

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## Details

- Name: Raca Enterprises, Inc. dba Life Cycle Herbal Products
- FEI Number: 3003858180
- City: El Monte
- State: California
- Country Name: United States
- Address Line 1: 2746 Durfee Ave Ste K
- Zip Code: 91732

## Related Documents

- [FDA Inspection 958333 - Raca Enterprises, Inc. dba Life Cycle Herbal Products - 2016-01-22](https://www.keypedia.com/records/fda_inspections/raca-enterprises-inc-dba-life-cycle-herbal-products/a72c0da7-0b84-4c90-97f4-bdcfa7580532) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 22, 2016
- [FDA Inspection 909519 - Raca Enterprises, Inc. dba Life Cycle Herbal Products - 2014-12-04](https://www.keypedia.com/records/fda_inspections/raca-enterprises-inc-dba-life-cycle-herbal-products/196b39c8-ed42-4540-8cd0-f4938ec05983) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 4, 2014
- [FDA Inspection 848592 - Raca Enterprises, Inc. dba Life Cycle Herbal Products - 2013-09-23](https://www.keypedia.com/records/fda_inspections/raca-enterprises-inc-dba-life-cycle-herbal-products/646ba1e5-a149-4078-aaea-2243d0322c23) — classification: Official Action Indicated (OAI), source: FDA, date: September 23, 2013
- [WARNING_LETTER - Raca Enterprises, Inc. dba Life Cycle Herbal Products - 2012-08-20](https://www.keypedia.com/records/warning_letter/raca-enterprises-inc-dba-life-cycle-herbal-products/981a8c58-c2e2-4305-95b0-9fb386564d16) — source: FDA, date: August 20, 2012
- [FDA Inspection 794818 - Raca Enterprises, Inc. dba Life Cycle Herbal Products - 2012-08-20](https://www.keypedia.com/records/fda_inspections/raca-enterprises-inc-dba-life-cycle-herbal-products/a8ec047a-8734-4397-a233-421a028a483f) — classification: Official Action Indicated (OAI), source: FDA, date: August 20, 2012

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