# FDA Inspection 660005 - Interdent Poland - April 10, 2010

Source: https://www.keypedia.com/records/fda_inspections/interdent-poland/39e322bc-88cf-496a-95be-3cc64067be4e
Source feed: FDA_Inspections

> FDA Inspection 660005 for Interdent Poland on April 10, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 660005
- Company Name: Interdent Poland
- Inspection Date: 2010-04-10
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/interdent-poland/6c4ee24b-8a14-4229-a99d-54ab0b81d08d

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