# FDA Inspection 684563 - Nutek Corporation of California - October 08, 2010

Source: https://www.keypedia.com/records/fda_inspections/nutek-corporation-of-california/07d5ec7a-3af0-4c5b-b110-ee1eef0d18fe
Source feed: FDA_Inspections

> FDA Inspection 684563 for Nutek Corporation of California on October 08, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 684563
- Company Name: Nutek Corporation of California
- Inspection Date: 2010-10-08
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 780826 - 2012-05-16](https://www.keypedia.com/records/fda_inspections/nutek-corporation-of-california/63e8a7bd-b5d8-4171-85f9-565f023dc8ba)
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- [FDA Inspection 684563 - 2010-10-08](https://www.keypedia.com/records/fda_inspections/nutek-corporation-of-california/20b06979-3348-49e4-948b-9eb424f72d74)

Company: https://www.keypedia.com/companies/nutek-corporation-of-california/c37b395f-f20c-4e75-86af-0619e324e2c5

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