# FDA Inspection 791722 - Myotronics-Noromed Inc - July 24, 2012

Source: https://www.keypedia.com/records/fda_inspections/myotronics-noromed-inc/f5f1f9c6-2010-4e18-9099-4e426982ef26
Source feed: FDA_Inspections

> FDA Inspection 791722 for Myotronics-Noromed Inc on July 24, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 791722
- Company Name: Myotronics-Noromed Inc
- Inspection Date: 2012-07-24
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/myotronics-noromed-inc/443158e1-852d-4efb-a948-8cb4f059e65a

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