FDA Inspection
ALR Technologies, Inc.ALR Technologies, Inc. – FDA Inspection, Aug 15, 2013
Record Details
This FDA Inspection record concerns ALR Technologies, Inc., with an inspection on August 15, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- ALR Technologies, Inc.
- Inspection Date
- August 15, 2013
- Product Type
- Devices
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ID · 8fa9002f-ca81-4868-8632-f7887f040ea9
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 844663
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.100(b)Documentation
- 21 CFR 820.30(a)Design control - no procedures
- 21 CFR 820.50(a)(2)Supplier oversight
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Other FDA inspections of ALR Technologies, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| March 22, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for ALR Technologies, Inc.
- FDA Inspection 966726 - 2016-03-22
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