# MVAP Medical Supplies, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/mvap-medical-supplies-inc/4e493684-c1ae-4ccb-b0df-c19722b7a0c6

> Inspection records and compliance data for MVAP Medical Supplies, Inc. in Thousand Oaks, California. Access full analysis and detailed observations.

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## Details

- Name: MVAP Medical Supplies, Inc.
- FEI Number: 3004622056
- City: Thousand Oaks
- State: California
- Country Name: United States
- Address Line 1: 2001 Corporate Center Dr
- Zip Code: 91320

## Related Documents

- [FDA Inspection 1196814 - MVAP Medical Supplies, Inc. - 2023-02-02](https://www.keypedia.com/records/fda_inspections/mvap-medical-supplies-inc/8f79993a-0813-420e-bf77-47f343485335) — classification: No Action Indicated (NAI), source: FDA, date: February 2, 2023
- [FDA Inspection 1196814 - MVAP Medical Supplies, Inc. - 2023-02-02](https://www.keypedia.com/records/fda_inspections/mvap-medical-supplies-inc/8af56e6f-d566-47a8-b11b-66caf4e34156) — classification: No Action Indicated (NAI), source: FDA, date: February 2, 2023
- [FDA Inspection 989543 - MVAP Medical Supplies, Inc. - 2016-09-06](https://www.keypedia.com/records/fda_inspections/mvap-medical-supplies-inc/954f11a4-dd83-4b27-afaf-3408615224a8) — classification: No Action Indicated (NAI), source: FDA, date: September 6, 2016
- [FDA Inspection 989543 - MVAP Medical Supplies, Inc. - 2016-09-06](https://www.keypedia.com/records/fda_inspections/mvap-medical-supplies-inc/b9e07087-337b-4839-ae74-3444ec5495bf) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 6, 2016
- [FDA Inspection 780133 - MVAP Medical Supplies, Inc. - 2012-05-02](https://www.keypedia.com/records/fda_inspections/mvap-medical-supplies-inc/656cfefe-4d16-420c-9d8c-b6b59715bb64) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 2, 2012
- [FDA Inspection 780133 - MVAP Medical Supplies, Inc. - 2012-05-02](https://www.keypedia.com/records/fda_inspections/mvap-medical-supplies-inc/1e501c6d-56d0-405c-aa39-849c765c9baa) — classification: No Action Indicated (NAI), source: FDA, date: May 2, 2012

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