FDA Inspection
Deringer-Ney, Inc.Deringer-Ney, Inc. – FDA Inspection, Feb 12, 2014
Record Details
This FDA Inspection record concerns Deringer-Ney, Inc., with an inspection on February 12, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Deringer-Ney, Inc.
- Inspection Date
- February 12, 2014
- Product Type
- Devices
View Company Profile
ID · 98ad9154-4fd4-44ff-9715-25f73ee30b3b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 871476
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.120Lack of or inadequate procedures for labeling
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Deringer-Ney, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| April 12, 2019 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 12, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Deringer-Ney, Inc.
- FDA Inspection 1086270 - 2019-04-12
- FDA Inspection 734145 - 2011-07-12
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