FDA Inspection
Remel Europe Ltd.Remel Europe Ltd. – FDA Inspection, Feb 11, 2016
Record Details
This FDA Inspection record concerns Remel Europe Ltd., with an inspection on February 11, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Remel Europe Ltd.
- Inspection Date
- February 11, 2016
- Product Type
- Devices
View Company Profile
ID · 4adc6293-b298-482d-bd9b-dfabdcd47034
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 961738
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Remel Europe Ltd.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| April 4, 2019 | Not classified | Office of Inspections and Investigations | |
| May 31, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 9, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Remel Europe Ltd.
- FDA Inspection 1116790 - 2019-04-04
- FDA Inspection 840261 - 2013-05-31
- FDA Inspection 580616 - 2009-04-09
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