FDA Inspection
Beevers Manufacturing & Supply, Inc.Beevers Manufacturing & Supply, Inc. – FDA Inspection, Jul 7, 2014
Record Details
This FDA Inspection record concerns Beevers Manufacturing & Supply, Inc., with an inspection on July 7, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- July 7, 2014
- Product Type
- Devices
View Company Profile
ID · a96719df-3665-4c86-ab99-01778f83c675
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 885368
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
9- 21 CFR 820.198(c)Investigation of device failures
- 21 CFR 820.20(c)Management review - defined interval, sufficient frequency
- 21 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.184Lack of or inadequate DHR procedures
- 21 CFR 820.80(d)Lack of or inadequate final acceptance procedures
- 21 CFR 820.22Quality audits - Lack of or inadequate procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
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