FDA Inspection
Organ Recovery Systems, Inc.Organ Recovery Systems, Inc. – FDA Inspection, Dec 9, 2009
Record Details
This FDA Inspection record concerns Organ Recovery Systems, Inc., with an inspection on December 9, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Organ Recovery Systems, Inc.
- Inspection Date
- December 9, 2009
- Product Type
- Devices
View Company Profile
ID · 30caded6-b297-4801-a109-0aeda841326d
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 634996
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Organ Recovery Systems, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| October 16, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 10, 2017 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 7, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 8, 2011 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Organ Recovery Systems, Inc.
- FDA Inspection 1071339 - 2018-10-16
- FDA Inspection 1001720 - 2017-02-10
- FDA Inspection 921541 - 2015-04-07
- FDA Inspection 752701 - 2011-11-08
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