FDA Inspection
Hubei Haixin Protective Product Group Co., Ltd.Hubei Haixin Protective Product Group Co., Ltd. – FDA Inspection, Dec 15, 2016
Record Details
This FDA Inspection record concerns Hubei Haixin Protective Product Group Co., Ltd., with an inspection on December 15, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- December 15, 2016
- Product Type
- Devices
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ID · f3f3d287-b371-4cc9-b376-3ce0e6583d61
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 996480
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 820.180Availability
- 21 CFR 820.75(b)Lack/Inad procedure-Monitoring/Control of Validated Proces
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
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