FDA Inspection
Myotronics-Noromed IncMyotronics-Noromed Inc – FDA Inspection, May 12, 2011
Record Details
This FDA Inspection record concerns Myotronics-Noromed Inc, with an inspection on May 12, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Myotronics-Noromed Inc
- Inspection Date
- May 12, 2011
- Product Type
- Devices
View Company Profile
ID · 4c104169-b58f-4b46-ae90-77eba0ac86db
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 722813
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Myotronics-Noromed Inc
5| Date | Classification | Office | Project area |
|---|---|---|---|
| December 5, 2018 | Not classified | Seattle District Office | |
| March 15, 2017 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| November 20, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 24, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 3, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Myotronics-Noromed Inc
- FDA Inspection 1096366 - 2018-12-05
- FDA Inspection 1008080 - 2017-03-15
- FDA Inspection 855812 - 2013-11-20
- FDA Inspection 791722 - 2012-07-24
- FDA Inspection 620293 - 2009-09-03
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