FDA Inspection
Cogmedix, Inc.Cogmedix, Inc. – FDA Inspection, May 31, 2013
Record Details
This FDA Inspection record concerns Cogmedix, Inc., with an inspection on May 31, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Cogmedix, Inc.
- Inspection Date
- May 31, 2013
- Product Type
- Devices
View Company Profile
ID · d624b2cf-ab94-4936-9d6f-93f17f5e2115
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 834006
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.100(a)Lack of or inadequate procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Cogmedix, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| April 11, 2024 | VAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| January 19, 2018 | Not classified | New England District Office | |
| April 21, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Cogmedix, Inc.
- FDA Inspection 1235696 - 2024-04-11
- FDA Inspection 1038648 - 2018-01-19
- FDA Inspection 722907 - 2011-04-21
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