# Winneram International Inc - Inspection Records

Source: https://www.keypedia.com/companies/winneram-international-inc/f46101c6-0a9d-406b-bbbc-2df05942be7b

> Inspection records and compliance data for Winneram International Inc in South El Monte, California. Access full analysis and detailed observations.

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## Details

- Name: Winneram International Inc
- FEI Number: 3001967145
- City: South El Monte
- State: California
- Country Name: United States
- Address Line 1: 1860 Tyler Ave
- Zip Code: 91733

## Related Documents

- [FDA Inspection 1230557 - Winneram International Inc - 2024-02-01](https://www.keypedia.com/records/fda_inspections/winneram-international-inc/266d3e3e-186b-41a3-9c9e-51b755c2f543) — classification: No Action Indicated (NAI), source: FDA, date: February 1, 2024
- [FDA Inspection 1123708 - Winneram International Inc - 2020-04-29](https://www.keypedia.com/records/fda_inspections/winneram-international-inc/eba1d58d-e4a6-43de-b6de-e00edbfa3a9c) — classification: No Action Indicated (NAI), source: FDA, date: April 29, 2020
- [FDA Inspection 1029494 - Winneram International Inc - 2017-08-30](https://www.keypedia.com/records/fda_inspections/winneram-international-inc/c1078fc4-3e35-457e-8566-f733e8af5eb1) — classification: No Action Indicated (NAI), source: FDA, date: August 30, 2017
- [FDA Inspection 1022866 - Winneram International Inc - 2017-08-23](https://www.keypedia.com/records/fda_inspections/winneram-international-inc/1cb77425-1858-4111-8cef-5df95f546daa) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 23, 2017
- [FDA Inspection 973561 - Winneram International Inc - 2016-06-03](https://www.keypedia.com/records/fda_inspections/winneram-international-inc/c22883fa-77e6-4c72-a1df-08bf13304d54) — classification: No Action Indicated (NAI), source: FDA, date: June 3, 2016
- [FDA Inspection 655043 - Winneram International Inc - 2010-03-01](https://www.keypedia.com/records/fda_inspections/winneram-international-inc/b648644d-97f0-42d2-9973-e7d026448c27) — classification: No Action Indicated (NAI), source: FDA, date: March 1, 2010

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