# FDA Inspection 562921 - Konigsberg Instruments Inc - February 02, 2009

Source: https://www.keypedia.com/records/fda_inspections/konigsberg-instruments-inc/d8d97db5-6bf2-4ef3-acd2-5ed7fe24825f
Source feed: FDA_Inspections

> FDA Inspection 562921 for Konigsberg Instruments Inc on February 02, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 562921
- Company Name: Konigsberg Instruments Inc
- Inspection Date: 2009-02-02
- 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 820692 - 2013-02-28](https://www.keypedia.com/records/fda_inspections/konigsberg-instruments-inc/0050fee1-22be-4203-91af-c2c81b322ab8)
- [FDA Inspection 820692 - 2013-02-28](https://www.keypedia.com/records/fda_inspections/konigsberg-instruments-inc/5fe61cce-4eda-4186-b18d-b1cf97202b63)
- [FDA Inspection 562921 - 2009-02-02](https://www.keypedia.com/records/fda_inspections/konigsberg-instruments-inc/f38274d7-06c8-4934-980e-32bf207d2d9c)

Company: https://www.keypedia.com/companies/konigsberg-instruments-inc/575fae7c-e239-4bc8-8d5c-c4d6820b34fe

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