FDA Inspection
Sanyo Tokyo Manufacturing Co., Ltd.Sanyo Tokyo Manufacturing Co., Ltd. – FDA Inspection, Jan 27, 2011
Record Details
This FDA Inspection record concerns Sanyo Tokyo Manufacturing Co., Ltd., with an inspection on January 27, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- January 27, 2011
- Product Type
- Devices
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ID · 976e633e-56e5-47ef-8ede-5cb63dece0b1
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 710527
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.120(d)Records, DHR {see also 820.184(e)}
- 21 CFR 820.90(b)(2)Product rework procedures, Lack of or inadequate procedures
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