FDA Inspection
Roche Molecular Systems, Inc.Roche Molecular Systems, Inc. – FDA Inspection, Oct 20, 2009
Record Details
This FDA Inspection record concerns Roche Molecular Systems, Inc., with an inspection on October 20, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- October 20, 2009
- Product Type
- Devices
View Company Profile
ID · 5b8f6684-2de7-4892-bcee-c366e1ff5b03
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 623869
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Roche Molecular Systems, Inc.
14| Date | Classification | Office | Project area |
|---|---|---|---|
| June 12, 2026 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| December 8, 2023 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| July 31, 2019 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| July 24, 2017 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| July 19, 2017 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Roche Molecular Systems, Inc.
- FDA Inspection 1323692 - 2026-06-12
- FDA Inspection 1224711 - 2023-12-08
- FDA Inspection 1100926 - 2019-07-31
- FDA Inspection 1027092 - 2017-07-24
- FDA Inspection 1020421 - 2017-07-19
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