# Herbalife Manufacturing, LLC, Lake Forest, CA – FDA Inspections

Source: https://www.keypedia.com/companies/herbalife-manufacturing-llc/a68d7b6f-1b3b-4056-bb5c-5fc68f8b0ddd

> Inspection records and compliance data for Herbalife Manufacturing, LLC in Lake Forest, California. 4 FDA inspections on record, last inspected May 04, 2022.

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## Details

- Name: Herbalife Manufacturing, LLC
- FEI Number: 3007696780
- Address Line 1: 20481 Crescent Bay Dr
- City: Lake Forest
- State: California
- Zip Code: 92630
- Country Name: United States
- Address: 20481 Crescent Bay Dr, Lake Forest, California 92630, United States
- Country: United States

## Related Documents

- FDA Inspection 1172134 - Herbalife Manufacturing, LLC - 2022-05-04 — classification: No Action Indicated (NAI), source: FDA, date: May 4, 2022
- FDA Inspection 1172134 - Herbalife Manufacturing, LLC - 2022-05-04 — classification: No Action Indicated (NAI), source: FDA, date: May 4, 2022
- FDA Inspection 1087085 - Herbalife Manufacturing, LLC - 2019-02-19 — classification: No Action Indicated (NAI), source: FDA, date: February 19, 2019
- FDA Inspection 1087085 - Herbalife Manufacturing, LLC - 2019-02-19 — classification: No Action Indicated (NAI), source: FDA, date: February 19, 2019
- [FDA Inspection 962514 - Herbalife Manufacturing, LLC - 2016-03-09](https://www.keypedia.com/records/fda_inspections/herbalife-manufacturing-llc/4eb63006-9f4f-48aa-9892-3d50af588b75) — classification: No Action Indicated (NAI), source: FDA, date: March 9, 2016
- FDA Inspection 962514 - Herbalife Manufacturing, LLC - 2016-03-09 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 9, 2016
- [FDA Inspection 849137 - Herbalife Manufacturing, LLC - 2013-09-11](https://www.keypedia.com/records/fda_inspections/herbalife-manufacturing-llc/a9ea3376-f7ab-4a5e-bf64-daaaac1df1e6) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 11, 2013
- FDA Inspection 849137 - Herbalife Manufacturing, LLC - 2013-09-11 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 11, 2013

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