FDA Inspection
Deerfield Imaging, Inc.Deerfield Imaging, Inc. – FDA Inspection, Oct 1, 2019
Record Details
This FDA Inspection record concerns Deerfield Imaging, Inc., with an inspection on October 1, 2019, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Deerfield Imaging, Inc.
- Inspection Date
- October 1, 2019
- Product Type
- Devices
View Company Profile
ID · ff8600cd-29a5-4a64-97fb-1662670bae18
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1106208
- FDA center
- Medical Devices & Rad Health
- Project area
- Radiation Control and Health Safety Act
FDA Citations
3- 21 CFR 1020.30(d)(1)Report of assembly submitted within 15 days
- 21 CFR 820.100(b)Documentation
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Deerfield Imaging, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| January 26, 2018 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| February 4, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Deerfield Imaging, Inc.
- FDA Inspection 1038905 - 2018-01-26
- FDA Inspection 913223 - 2015-02-04
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