FDA Inspection
Medtimo IncMedtimo Inc – FDA Inspection, May 4, 2016
Record Details
This FDA Inspection record concerns Medtimo Inc, with an inspection on May 4, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Medtimo Inc
- Inspection Date
- May 4, 2016
- Product Type
- Devices
View Company Profile
ID · 6036f5c4-a2f9-4202-ae8b-ab3c72271d6d
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 968712
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Medtimo Inc
6| Date | Classification | Office | Project area |
|---|---|---|---|
| February 15, 2018 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| November 13, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 3, 2016 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| January 23, 2015 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| June 18, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Medtimo Inc
- FDA Inspection 1041724 - 2018-02-15
- FDA Inspection 1035426 - 2017-11-13
- FDA Inspection 993558 - 2016-11-03
- FDA Inspection 912086 - 2015-01-23
- FDA Inspection 884334 - 2014-06-18
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