# Neolife International LLC, Hayward, CA – FDA Inspections

Source: https://www.keypedia.com/companies/neolife-international-llc/55ddeb8f-aeb4-4556-a77f-047dec8c4753

> Inspection records and compliance data for Neolife International LLC in Hayward, California. 5 FDA inspections on record, 1 Form 483, last inspected September 16, 2026.

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## Details

- Name: Neolife International LLC
- FEI Number: 2912990
- Address Line 1: 2125 American Ave
- City: Hayward
- State: California
- Zip Code: 94545
- Country Name: United States
- Address: 2125 American Ave, Hayward, California 94545, United States
- Country: United States

## Related Documents

- [FDA Inspection 1336268 - Neolife International LLC - 2026-09-16](https://www.keypedia.com/records/fda_inspections/neolife-international-llc/9ffdc7ec-1ae4-4c44-a216-7666552c9676) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 16, 2026
- FDA Inspection 1336268 - Neolife International LLC - 2026-09-16 — classification: No Action Indicated (NAI), source: FDA, date: September 16, 2026
- FDA Inspection 1122792 - Neolife International LLC - 2020-01-03 — classification: No Action Indicated (NAI), source: FDA, date: January 3, 2020
- FDA Inspection 1122792 - Neolife International LLC - 2020-01-03 — classification: No Action Indicated (NAI), source: FDA, date: January 3, 2020
- FDA Inspection 1022132 - Neolife International LLC - 2017-05-30 — classification: No Action Indicated (NAI), source: FDA, date: May 30, 2017
- FDA Inspection 881824 - Neolife International LLC - 2014-06-02 — classification: No Action Indicated (NAI), source: FDA, date: June 2, 2014
- FDA Inspection 881824 - Neolife International LLC - 2014-06-02 — classification: No Action Indicated (NAI), source: FDA, date: June 2, 2014
- [FDA Inspection 779201 - Neolife International LLC - 2012-04-20](https://www.keypedia.com/records/fda_inspections/neolife-international-llc/bdfc4fac-68e4-4b98-ab04-0ccfc28f46b6) — classification: No Action Indicated (NAI), source: FDA, date: April 20, 2012
- FDA Inspection 779201 - Neolife International LLC - 2012-04-20 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 20, 2012

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