# Motion Analysis Corporation, Santa Rosa, CA – FDA Inspections

Source: https://www.keypedia.com/companies/motion-analysis-corporation/47572528-a3a3-4c5e-9aea-def7e778034d

> Inspection records and compliance data for Motion Analysis Corporation in Santa Rosa, California. 4 FDA inspections on record, 2 Form 483s, last inspected July 21, 2017.

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## Details

- Name: Motion Analysis Corporation
- FEI Number: 2939117
- Address Line 1: 3617 Westwind Blvd
- City: Santa Rosa
- State: California
- Zip Code: 95403
- Country Name: United States
- Address: 3617 Westwind Blvd, Santa Rosa, California 95403, United States
- Country: United States

## Related Documents

- FDA Inspection 1018699 - Motion Analysis Corporation - 2017-07-21 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 21, 2017
- [FDA Inspection 1018699 - Motion Analysis Corporation - 2017-07-21](https://www.keypedia.com/records/fda_inspections/motion-analysis-corporation/7dfb2bbc-9e21-4a41-8994-4dd22463ea97) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 21, 2017
- FDA Inspection 1003151 - Motion Analysis Corporation - 2016-11-07 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 7, 2016
- [FDA Inspection 1003151 - Motion Analysis Corporation - 2016-11-07](https://www.keypedia.com/records/fda_inspections/motion-analysis-corporation/fd309947-24c3-4204-bc2e-9da957464f0a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 7, 2016
- [FDA Inspection 834109 - Motion Analysis Corporation - 2013-06-02](https://www.keypedia.com/records/fda_inspections/motion-analysis-corporation/28a5404b-d96f-4a76-ae35-139abea1dbac) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 2, 2013
- FDA Inspection 741250 - Motion Analysis Corporation - 2011-08-24 — classification: No Action Indicated (NAI), source: FDA, date: August 24, 2011
- FDA Inspection 741250 - Motion Analysis Corporation - 2011-08-24 — classification: No Action Indicated (NAI), source: FDA, date: August 24, 2011

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