FDA Inspection
Aalnex Inc.Aalnex Inc. – FDA Inspection, Jul 26, 2011
Record Details
This FDA Inspection record concerns Aalnex Inc., with an inspection on July 26, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Aalnex Inc.
- Inspection Date
- July 26, 2011
- Product Type
- Devices
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ID · 8abb5535-5759-4bfb-affd-6c009fbcb0e5
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 736182
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
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