FDA Inspection
Dentsply IH, Inc.Dentsply IH, Inc. – FDA Inspection, Mar 15, 2012
Record Details
This FDA Inspection record concerns Dentsply IH, Inc., with an inspection on March 15, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Dentsply IH, Inc.
- Inspection Date
- March 15, 2012
- Product Type
- Devices
View Company Profile
ID · 10223809-ab15-4ca8-af82-751631529595
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 775121
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.100(a)Lack of or inadequate procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Dentsply IH, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| August 30, 2018 | Not classified | New England District Office | |
| January 11, 2017 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| September 3, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Dentsply IH, Inc.
- FDA Inspection 1141451 - 2018-08-30
- FDA Inspection 997615 - 2017-01-11
- FDA Inspection 945200 - 2015-09-03
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