FDA Inspection
Alken Inc.Alken Inc. – FDA Inspection, Sep 12, 2017
Record Details
This FDA Inspection record concerns Alken Inc., with an inspection on September 12, 2017, issued by the Center for Devices and Radiological Health, covering devices.
- Person
- James W. Whitney (Issuing Officer)
View Company Profile
ID · a64e298e-920f-40d4-8817-1e5719ed458a
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1027428
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Alken Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| July 24, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 16, 2012 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| May 8, 2009 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
Other documents for Alken Inc.
- FDA Inspection 888714 - 2014-07-24
- FDA Inspection 767900 - 2012-02-16
- FDA Inspection 583580 - 2009-05-08
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