FDA Inspection
Beckman Coulter Inc.Beckman Coulter Inc. – FDA Inspection, Oct 6, 2017
Record Details
This FDA Inspection record concerns Beckman Coulter Inc., with an inspection on October 6, 2017, issued by the Los Angeles District Office, covering medical devices & rad health.
- Company
- Beckman Coulter Inc.
- Inspection Date
- October 6, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 6cd07c40-2d30-487f-bcce-391001e01837
Inspection Facts
- Inspection number
- 1052813
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Beckman Coulter Inc.
8| Date | Classification | Office | Project area |
|---|---|---|---|
| August 5, 2021 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 30, 2019 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 28, 2018 | Not classified | Los Angeles District Office | |
| July 16, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 12, 2011 | OAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Beckman Coulter Inc.
- FDA Inspection 1149891 - 2021-08-05
- FDA Inspection 1111029 - 2019-10-30
- FDA Inspection 1130186 - 2018-09-28
- FDA Inspection 791139 - 2012-07-16
- FDA Inspection 725062 - 2011-05-12
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