# MatOrtho Ltd - Inspection Records

Source: https://www.keypedia.com/companies/matortho-ltd/6151c514-3865-4737-9b65-a394e12197e6

> Inspection records and compliance data for MatOrtho Ltd in Leatherhead, None. Access full analysis and detailed observations.

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## Details

- Name: MatOrtho Ltd
- FEI Number: 3008985661
- City: Leatherhead
- State: None
- Country Name: United Kingdom
- Address Line 1: 19/20 Mole Business Park, Randalls Road
- Zip Code: None

## Related Documents

- [FDA Inspection 1191982 - MatOrtho Ltd - 2022-11-03](https://www.keypedia.com/records/fda_inspections/matortho-ltd/6e944178-4d6a-4ae4-b548-dfe6d3176495) — classification: No Action Indicated (NAI), source: FDA, date: November 3, 2022
- [FDA Inspection 1191982 - MatOrtho Ltd - 2022-11-03](https://www.keypedia.com/records/fda_inspections/matortho-ltd/1b3844aa-86a1-42a7-9fb7-cfbdea3f7ae1) — classification: No Action Indicated (NAI), source: FDA, date: November 3, 2022
- [483 - MatOrtho Ltd - 2020-03-05](https://www.keypedia.com/records/483/matortho-ltd/a0334aa3-c09d-4a24-9558-44811dde380c) — source: FDA, date: March 5, 2020
- [FDA Inspection 1120806 - MatOrtho Ltd - 2020-03-05](https://www.keypedia.com/records/fda_inspections/matortho-ltd/fb16c5d7-e08c-4d47-a560-27da182b9b6b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 5, 2020
- [FDA Inspection 1120806 - MatOrtho Ltd - 2020-03-05](https://www.keypedia.com/records/fda_inspections/matortho-ltd/660b9c72-8955-4338-be1f-e4c11eb4bc6a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 5, 2020
- [FDA Inspection 949343 - MatOrtho Ltd - 2015-10-22](https://www.keypedia.com/records/fda_inspections/matortho-ltd/af220d77-a28f-4616-bcea-3ea512ca6361) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 22, 2015
- [FDA Inspection 949343 - MatOrtho Ltd - 2015-10-22](https://www.keypedia.com/records/fda_inspections/matortho-ltd/cb3ad5ad-adbc-4ad5-8e03-d25f70403992) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 22, 2015

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