FDA Inspection
Prosurg, Inc.Prosurg, Inc. – FDA Inspection, Feb 2, 2018
Record Details
This FDA Inspection record concerns Prosurg, Inc., with an inspection on February 2, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · d745b5bc-4e14-41a6-a299-511ba6b5b24f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1039513
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.198(a)Complaints
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Prosurg, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| March 29, 2024 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 27, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 21, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 17, 2008 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Prosurg, Inc.
- FDA Inspection 1237927 - 2024-03-29
- FDA Inspection 901125 - 2014-10-27
- FDA Inspection 808124 - 2012-11-21
- FDA Inspection 542768 - 2008-10-17
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