FDA Inspection
Bruin Manufacturing Company, Inc.Bruin Manufacturing Company, Inc. – FDA Inspection, Jan 12, 2018
Record Details
This FDA Inspection record concerns Bruin Manufacturing Company, Inc., with an inspection on January 12, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 2081b5ec-08d5-4288-b6a4-e4e59011158c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1037621
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Bruin Manufacturing Company, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| November 20, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Bruin Manufacturing Company, Inc.
- FDA Inspection 904385 - 2014-11-20
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