FDA Inspection
Accutome, IncAccutome, Inc – FDA Inspection, Jul 3, 2018
Record Details
This FDA Inspection record concerns Accutome, Inc, with an inspection on July 3, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · f0bf7c62-a984-43ec-8223-bcacbe7f14e9
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1057783
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Accutome, Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| September 5, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 3, 2009 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Accutome, Inc
- FDA Inspection 894258 - 2014-09-05
- FDA Inspection 575624 - 2009-04-03
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