# Minaris Medical America, Inc. – FDA Inspection, Aug 6, 2010

Source: https://www.keypedia.com/records/fda_inspections/minaris-medical-america-inc/b83a9580-bb5d-481f-ba3d-87a63219f04c
Source feed: FDA_Inspections

> FDA inspection 675121 of Minaris Medical America, Inc., August 06, 2010. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 806 and 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 675121
- Company Name: Minaris Medical America, Inc.
- Inspection Date: 2010-08-06
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 1194876 - 2022-12-16](https://www.keypedia.com/records/fda_inspections/minaris-medical-america-inc/77e91fe9-be98-4560-b3cf-f250d44575ac)
- FDA Inspection 1097911 - 2019-06-06
- FDA Inspection 923042 - 2015-04-21
- FDA Inspection 792552 - 2012-07-11

Company: https://www.keypedia.com/companies/minaris-medical-america-inc/b1e8ef36-a25b-4de3-a82f-bb447850c207

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7