FDA Inspection
Togo Medikit Co., Ltd.Togo Medikit Co., Ltd. – FDA Inspection, Oct 14, 2011
Record Details
This FDA Inspection record concerns Togo Medikit Co., Ltd., with an inspection on October 14, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Togo Medikit Co., Ltd.
- Inspection Date
- October 14, 2011
- Product Type
- Devices
View Company Profile
ID · d159ef27-9980-4fc6-ae0f-e918e11f10d8
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 752942
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
3- 21 CFR 820.100(b)Documentation
- 21 CFR 820.25(b)Training records
- 21 CFR 820.70(c)Environmental control Lack of or inadequate procedures
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