FDA Inspection
Angiodynamics IncAngiodynamics Inc – FDA Inspection, Aug 24, 2015
Record Details
This FDA Inspection record concerns Angiodynamics Inc, with an inspection on August 24, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Angiodynamics Inc
- Inspection Date
- August 24, 2015
- Product Type
- Devices
View Company Profile
ID · a6944a2c-89f1-4043-93b2-61ef3eadc427
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 942381
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.198(a)General
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Angiodynamics Inc
7| Date | Classification | Office | Project area |
|---|---|---|---|
| September 26, 2018 | Not classified | New England District Office | |
| August 24, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 28, 2014 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 13, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 16, 2011 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
Other documents for Angiodynamics Inc
- FDA Inspection 1122886 - 2018-09-26
- FDA Inspection 942383 - 2015-08-24
- FDA Inspection 882250 - 2014-05-28
- FDA Inspection 764802 - 2012-02-13
- FDA Inspection 745689 - 2011-09-16
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