FDA Inspection
Beckman Coulter, Inc.Beckman Coulter, Inc. – FDA Inspection, Dec 8, 2017
Record Details
This FDA Inspection record concerns Beckman Coulter, Inc., with an inspection on December 8, 2017, issued by the Florida District Office, covering medical devices & rad health.
- Company
- Beckman Coulter, Inc.
- Inspection Date
- December 8, 2017
- Product Type
- Medical Devices & Rad Health
- Office
- Florida District Office
View Company Profile
ID · f45facf7-a59c-498a-bb5e-c1d1b6a05af5
Inspection Facts
- Inspection number
- 1081378
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Beckman Coulter, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| October 28, 2021 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 16, 2017 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 11, 2013 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 2, 2011 | OAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Beckman Coulter, Inc.
- FDA Inspection 1155995 - 2021-10-28
- FDA Inspection 1028860 - 2017-10-16
- FDA Inspection 848046 - 2013-09-11
- FDA Inspection 729388 - 2011-06-02
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