FDA Inspection
International Immuno-Diagnostics Inc.International Immuno-Diagnostics Inc. – FDA Inspection, Jan 23, 2012
Record Details
This FDA Inspection record concerns International Immuno-Diagnostics Inc., with an inspection on January 23, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- January 23, 2012
- Product Type
- Devices
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ID · dcae2fef-c240-4cb1-8332-9093a369409f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 764800
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
2- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
- 21 CFR 806.20(a)Records not kept
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Other FDA inspections of International Immuno-Diagnostics Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| March 31, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| January 3, 2011 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 18, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 7, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for International Immuno-Diagnostics Inc.
- FDA Inspection 920347 - 2015-03-31
- FDA Inspection 701858 - 2011-01-03
- FDA Inspection 663760 - 2010-05-18
- FDA Inspection 542096 - 2009-01-07
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