FDA Inspection
Myotronics-Noromed IncMyotronics-Noromed Inc – FDA Inspection, Dec 5, 2018
Record Details
This FDA Inspection record concerns Myotronics-Noromed Inc, with an inspection on December 5, 2018, issued by the Seattle District Office, covering medical devices & rad health.
- Company
- Myotronics-Noromed Inc
- Inspection Date
- December 5, 2018
- Product Type
- Medical Devices & Rad Health
- Office
- Seattle District Office
View Company Profile
ID · 8cbd2c58-f93e-4418-a5c6-3d2366555549
Inspection Facts
- Inspection number
- 1096366
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Myotronics-Noromed Inc
5| Date | Classification | Office | Project area |
|---|---|---|---|
| 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 |
| May 12, 2011 | OAI | 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 1008080 - 2017-03-15
- FDA Inspection 855812 - 2013-11-20
- FDA Inspection 791722 - 2012-07-24
- FDA Inspection 722813 - 2011-05-12
- FDA Inspection 620293 - 2009-09-03
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