FDA Inspection
Euroimmun US, Inc.Euroimmun US, Inc. – FDA Inspection, Sep 6, 2019
Record Details
This FDA Inspection record concerns Euroimmun US, Inc., with an inspection on September 6, 2019, issued by the New Jersey District Office, covering medical devices & rad health.
- Company
- Euroimmun US, Inc.
- Inspection Date
- September 6, 2019
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 642f8da5-c163-4bae-93e7-eaa88ecd24eb
Inspection Facts
- Inspection number
- 1123894
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Euroimmun US, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| November 13, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 13, 2011 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| August 31, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 26, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Euroimmun US, Inc.
- FDA Inspection 906754 - 2014-11-13
- FDA Inspection 756874 - 2011-12-13
- FDA Inspection 611478 - 2009-08-31
- FDA Inspection 610980 - 2009-08-26
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