FDA Inspection
Remel Europe Ltd.Remel Europe Ltd. – FDA Inspection, Apr 4, 2019
Record Details
This FDA Inspection record concerns Remel Europe Ltd., with an inspection on April 4, 2019, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Company
- Remel Europe Ltd.
- Inspection Date
- April 4, 2019
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · a4a99b81-77e9-4448-b3f3-e19826ce71f3
Inspection Facts
- Inspection number
- 1116790
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Remel Europe Ltd.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| February 11, 2016 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| 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 961738 - 2016-02-11
- FDA Inspection 840261 - 2013-05-31
- FDA Inspection 580616 - 2009-04-09
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