FDA Inspection
Shenzhen Creative Industry Co., Ltd.Shenzhen Creative Industry Co., Ltd. – FDA Inspection, Jun 7, 2012
Record Details
This FDA Inspection record concerns Shenzhen Creative Industry Co., Ltd., with an inspection on June 7, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- June 7, 2012
- Product Type
- Devices
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ID · b67a8586-ae33-4cab-a534-bf15e2fc3713
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 790430
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.30(f)Design verification - Lack of or inadequate procedures
- 21 CFR 820.80(d)Lack of or inadequate final acceptance procedures
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Other FDA inspections of Shenzhen Creative Industry Co., Ltd.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| November 8, 2018 | Not classified | Office of Inspections and Investigations | |
| August 6, 2015 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Shenzhen Creative Industry Co., Ltd.
- FDA Inspection 1082638 - 2018-11-08
- FDA Inspection 940774 - 2015-08-06
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