# FDA Inspection 563969 - Neurotron Medical Inc. - February 23, 2009

Source: https://www.keypedia.com/records/fda_inspections/neurotron-medical-inc/afc418cd-19f0-4db8-a4b5-67126e7160eb
Source feed: FDA_Inspections

> FDA Inspection 563969 for Neurotron Medical Inc. on February 23, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 563969
- Company Name: Neurotron Medical Inc.
- Inspection Date: 2009-02-23
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/neurotron-medical-inc/cd8284f1-104b-48f5-aa72-392469492da6

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