FDA Inspection
Unfors RaySafe ABUnfors RaySafe AB – FDA Inspection, Sep 3, 2014
Record Details
This FDA Inspection record concerns Unfors RaySafe AB, with an inspection on September 3, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Unfors RaySafe AB
- Inspection Date
- September 3, 2014
- Product Type
- Devices
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ID · 58ec42ac-628c-4999-a1b7-72c7f51ea617
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 893811
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 803.17Lack of Written MDR Procedures
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