FDA Inspection
Randox Laboratories, LimitedRandox Laboratories, Limited – FDA Inspection, Apr 28, 2016
Record Details
This FDA Inspection record concerns Randox Laboratories, Limited, with an inspection on April 28, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Randox Laboratories, Limited
- Inspection Date
- April 28, 2016
- Product Type
- Devices
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ID · 4fe2b409-5e0a-4615-8336-6b5e2f56d44e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 969542
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
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