FDA Inspection
Bio-Rad Laboratories, Inc.Bio-Rad Laboratories, Inc. – FDA Inspection, Jul 8, 2011
Record Details
This FDA Inspection record concerns Bio-Rad Laboratories, Inc., with an inspection on July 8, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Bio-Rad Laboratories, Inc.
- Inspection Date
- July 8, 2011
- Product Type
- Devices
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ID · 3a414078-bc07-4aa4-b887-922550923537
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 733170
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 806.10(b)Time to report - 10 days
- 21 CFR 820.198(c)Investigation of device failures
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Other FDA inspections of Bio-Rad Laboratories, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| August 17, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 25, 2016 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 10, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Bio-Rad Laboratories, Inc.
- FDA Inspection 1026651 - 2017-08-17
- FDA Inspection 975116 - 2016-02-25
- FDA Inspection 832958 - 2013-07-10
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