FDA Inspection
Medi-Source IncMedi-Source Inc – FDA Inspection, Jul 11, 2017
Record Details
This FDA Inspection record concerns Medi-Source Inc, with an inspection on July 11, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · d042c933-f1f8-4f8d-8bd8-b181fcde5006
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1017923
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
- 21 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
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Other FDA inspections of Medi-Source Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| April 13, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| July 23, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Medi-Source Inc
- FDA Inspection 922180 - 2015-04-13
- FDA Inspection 673049 - 2010-07-23
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