FDA Inspection
AngioDynamics, Inc.AngioDynamics, Inc. – FDA Inspection, May 27, 2010
Record Details
This FDA Inspection record concerns AngioDynamics, Inc., with an inspection on May 27, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- AngioDynamics, Inc.
- Inspection Date
- May 27, 2010
- Product Type
- Devices
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ID · f0159826-4db8-453a-8c07-0e3ebfa737c3
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 663044
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
1- 21 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
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Other FDA inspections of AngioDynamics, Inc.
9| Date | Classification | Office | Project area |
|---|---|---|---|
| June 25, 2021 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| April 15, 2016 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| August 13, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 15, 2014 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 30, 2014 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for AngioDynamics, Inc.
- FDA Inspection 1145201 - 2021-06-25
- FDA Inspection 967909 - 2016-04-15
- FDA Inspection 941614 - 2015-08-13
- FDA Inspection 887029 - 2014-07-15
- FDA Inspection 866897 - 2014-03-30
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