# FDA Inspection 552454 - EM Probe, Inc. - November 04, 2008

Source: https://www.keypedia.com/records/fda_inspections/em-probe-inc/ee286c76-ae42-4922-9f79-e7716131e72b
Source feed: FDA_Inspections

> FDA Inspection 552454 for EM Probe, Inc. on November 04, 2008. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 552454
- Company Name: EM Probe, Inc.
- Inspection Date: 2008-11-04
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 552454 - 2008-11-04](https://www.keypedia.com/records/fda_inspections/em-probe-inc/10ffed2e-919c-4af5-ae14-c361f07a748c)

Company: https://www.keypedia.com/companies/em-probe-inc/7b531938-fe38-4630-8d28-d203f1dc0dd3

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