# Myotronics-Noromed Inc – FDA Inspection, May 12, 2011

Source: https://www.keypedia.com/records/fda_inspections/myotronics-noromed-inc/4c104169-b58f-4b46-ae90-77eba0ac86db
Source feed: FDA_Inspections

> FDA inspection 722813 of Myotronics-Noromed Inc, May 12, 2011. Classification: Official Action Indicated (OAI). 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 722813
- Company Name: Myotronics-Noromed Inc
- Inspection Date: 2011-05-12
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1096366 - 2018-12-05](https://www.keypedia.com/records/fda_inspections/myotronics-noromed-inc/8cbd2c58-f93e-4418-a5c6-3d2366555549)
- FDA Inspection 1008080 - 2017-03-15
- FDA Inspection 855812 - 2013-11-20
- FDA Inspection 791722 - 2012-07-24
- FDA Inspection 620293 - 2009-09-03

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