# FDA Inspection 574853 - Interdent, Inc. - March 05, 2009

Source: https://www.keypedia.com/records/fda_inspections/interdent-inc/3d213eb8-74ae-483f-8d43-05b53c845ade
Source feed: FDA_Inspections

> FDA Inspection 574853 for Interdent, Inc. on March 05, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 574853
- Company Name: Interdent, Inc.
- Inspection Date: 2009-03-05
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 574853 - 2009-03-05](https://www.keypedia.com/records/fda_inspections/interdent-inc/2f93bf27-24e4-47ab-90d8-76ac2e7cf563)

Company: https://www.keypedia.com/companies/interdent-inc/0add5be0-59f0-4fc1-9a17-330fd87c6804

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