FDA Inspection
Merz North America, Inc.Merz North America, Inc. – FDA Inspection, Apr 19, 2013
Record Details
This FDA Inspection record concerns Merz North America, Inc., with an inspection on April 19, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Merz North America, Inc.
- Inspection Date
- April 19, 2013
- Product Type
- Devices
View Company Profile
ID · d5bca3e3-884d-4e8b-a09e-4a0b75c25fe5
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 834443
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
Other FDA inspections of Merz North America, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| May 25, 2017 | Not classified | Minneapolis District Office | |
| September 2, 2014 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| April 8, 2011 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 23, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Merz North America, Inc.
- FDA Inspection 1034616 - 2017-05-25
- FDA Inspection 893657 - 2014-09-02
- FDA Inspection 715962 - 2011-04-08
- FDA Inspection 702452 - 2010-12-23
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