FDA Inspection
Alcor Scientific, Inc.Alcor Scientific, Inc. – FDA Inspection, Mar 30, 2011
Record Details
This FDA Inspection record concerns Alcor Scientific, Inc., with an inspection on March 30, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Alcor Scientific, Inc.
- Inspection Date
- March 30, 2011
- Product Type
- Devices
View Company Profile
ID · 2c8ac348-071e-478b-99fc-fd8fad3da477
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 718263
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.80(e)Documentation
- 21 CFR 820.40Lack of procedures, or not maintained
- 21 CFR 820.150Lack of or inadequate procedures for storage.
- 21 CFR 820.198(e)Records of complaint investigation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Alcor Scientific, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| December 18, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 9, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 31, 2009 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Alcor Scientific, Inc.
- FDA Inspection 1074839 - 2018-12-18
- FDA Inspection 782014 - 2012-05-09
- FDA Inspection 638618 - 2009-12-31
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