# FDA Inspection 1088552 - The Metrix Company - April 25, 2019

Source: https://www.keypedia.com/records/fda_inspections/the-metrix-company/afa04e4c-1612-44b2-9619-90ae1124305f
Source feed: FDA_Inspections

> FDA inspection 1088552 of The Metrix Company, April 25, 2019. Classification: Voluntary Action Indicated (VAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1088552
- Company Name: The Metrix Company
- Inspection Date: 2019-04-25
- 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: 0

## Related Documents

- [FDA Inspection 969394 - 2016-05-06](https://www.keypedia.com/records/fda_inspections/the-metrix-company/a06abbdd-4658-4578-838e-6df1add924c7)
- FDA Inspection 886826 - 2014-07-09
- FDA Inspection 662262 - 2010-04-22

Company: https://www.keypedia.com/companies/the-metrix-company/02c0379f-f348-448b-8670-558a226c9829

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