# FDA Inspection 839521 - Centrix, Inc. - June 27, 2013

Source: https://www.keypedia.com/records/fda_inspections/centrix-inc/9f9f1b81-150e-43c9-b91b-8aec7dcf5f31
Source feed: FDA_Inspections

> FDA Inspection 839521 for Centrix, Inc. on June 27, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 839521
- Company Name: Centrix, Inc.
- Inspection Date: 2013-06-27
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/centrix-inc/f67d1354-9497-4a39-9320-0be314e62568

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