FDA Inspection
HiJax Productions - Jonathan A. NorlingHiJax Productions - Jonathan A. Norling – FDA Inspection, Oct 12, 2011
Record Details
This FDA Inspection record concerns HiJax Productions - Jonathan A. Norling, with an inspection on October 12, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- October 12, 2011
- Product Type
- Devices
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ID · 55d1caac-b0a6-460a-b2be-b817c4343252
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 739838
- FDA center
- Medical Devices & Rad Health
- Project area
- Radiation Control and Health Safety Act
FDA Citations
1- 21 CFR 1040.11(c)Demonstration laser products
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