# J.M Huber Micropowders, Inc - Inspection Records

Source: https://www.keypedia.com/companies/jm-huber-micropowders-inc/29e05493-3c2b-4d4b-ac8d-da0ba1cefba8

> Inspection records and compliance data for J.M Huber Micropowders, Inc in La Mirada, California. Access full analysis and detailed observations.

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## Details

- Name: J.M Huber Micropowders, Inc
- FEI Number: 3003665718
- City: La Mirada
- State: California
- Country Name: United States
- Address Line 1: 16024 Phoebe Ave
- Zip Code: 90638

## Related Documents

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- [FDA Inspection 1032048 - J.M Huber Micropowders, Inc - 2017-10-23](https://www.keypedia.com/records/fda_inspections/jm-huber-micropowders-inc/5f935afa-f561-4126-a402-8796e3935b06) — classification: No Action Indicated (NAI), source: FDA, date: October 23, 2017
- [FDA Inspection 1032048 - J.M Huber Micropowders, Inc - 2017-10-23](https://www.keypedia.com/records/fda_inspections/jm-huber-micropowders-inc/39236dc8-e897-4855-98b7-09159235393b) — classification: No Action Indicated (NAI), source: FDA, date: October 23, 2017
- [FDA Inspection 902503 - J.M Huber Micropowders, Inc - 2014-10-30](https://www.keypedia.com/records/fda_inspections/jm-huber-micropowders-inc/4f19ccf4-e59f-48ca-a550-6de237b60ceb) — classification: No Action Indicated (NAI), source: FDA, date: October 30, 2014
- [FDA Inspection 902503 - J.M Huber Micropowders, Inc - 2014-10-30](https://www.keypedia.com/records/fda_inspections/jm-huber-micropowders-inc/7b86b550-b18f-4975-819a-bd32c8d39c7e) — classification: No Action Indicated (NAI), source: FDA, date: October 30, 2014
- [FDA Inspection 763322 - J.M Huber Micropowders, Inc - 2012-01-18](https://www.keypedia.com/records/fda_inspections/jm-huber-micropowders-inc/d716f56e-fdad-4194-b5bc-15e717f520df) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 18, 2012
- [FDA Inspection 763322 - J.M Huber Micropowders, Inc - 2012-01-18](https://www.keypedia.com/records/fda_inspections/jm-huber-micropowders-inc/99955806-cc66-4bf6-9188-f9b61beef132) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 18, 2012

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