FDA Inspection
Circadiance LLCCircadiance LLC – FDA Inspection, Apr 7, 2017
Record Details
This FDA Inspection record concerns Circadiance LLC, with an inspection on April 7, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · a1197094-fc31-42d2-99fd-a1246b3d0bf7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1010778
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Circadiance LLC
5| Date | Classification | Office | Project area |
|---|---|---|---|
| August 30, 2024 | Not classified | Philadelphia District Office | Compliance: Devices |
| March 20, 2019 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 30, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 16, 2011 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| April 1, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Circadiance LLC
- FDA Inspection 1235615 - 2024-08-30
- FDA Inspection 1098418 - 2019-03-20
- FDA Inspection 816321 - 2013-01-30
- FDA Inspection 709921 - 2011-02-16
- FDA Inspection 572951 - 2009-04-01
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