FDA Inspection
Cardinal Health Mexico 244 S de RL de CVCardinal Health Mexico 244 S de RL de CV – FDA Inspection, Feb 12, 2016
Record Details
This FDA Inspection record concerns Cardinal Health Mexico 244 S de RL de CV, with an inspection on February 12, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- February 12, 2016
- Product Type
- Devices
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ID · 8735ad9a-9f58-42b9-a88c-03221eb1d872
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 962206
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.75(a)Lack of or inadequate process validation
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
- 21 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
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Other FDA inspections of Cardinal Health Mexico 244 S de RL de CV
2| Date | Classification | Office | Project area |
|---|---|---|---|
| April 3, 2014 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| July 30, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Cardinal Health Mexico 244 S de RL de CV
- FDA Inspection 879354 - 2014-04-03
- FDA Inspection 611033 - 2009-07-30
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