FDA Inspection
Tianjin MasterVision Technology Co., Ltd.Tianjin MasterVision Technology Co., Ltd. – FDA Inspection, Aug 31, 2023
Record Details
This FDA Inspection record concerns Tianjin MasterVision Technology Co., Ltd., with an inspection on August 31, 2023, issued by the Office of Inspections and Investigations.
- Inspection Date
- August 31, 2023
View Company Profile
ID · db415169-f48b-4ca7-98d5-f9274a6fa460
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1218181
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
FDA Citations
4- 21 CFR 820.100(b)Documentation
- 21 CFR 820.30(f)Design verification - Lack of or inadequate procedures
- 21 CFR 820.50(a)(2)Supplier oversight
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
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