# FDA Inspection 596999 - Carematix, Inc. - July 14, 2009

Source: https://www.keypedia.com/records/fda_inspections/carematix-inc/e360a91b-bbc8-49f8-b112-05a98b53c488
Source feed: FDA_Inspections

> FDA Inspection 596999 for Carematix, Inc. on July 14, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 596999
- Company Name: Carematix, Inc.
- Inspection Date: 2009-07-14
- Classification: Voluntary Action Indicated (VAI)
- 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/carematix-inc/3e65a3e8-a57d-49f6-a800-792dc44ee529

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