FDA Inspection
Flextronics Medical Device Manufacturing(Shenzhen) Co., Ltd.Flextronics Medical Device Manufacturing(Shenzhen) Co., Ltd. – FDA Inspection, Aug 26, 2010
Record Details
This FDA Inspection record concerns Flextronics Medical Device Manufacturing(Shenzhen) Co., Ltd., with an inspection on August 26, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- August 26, 2010
- Product Type
- Devices
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ID · 4c73e953-84e5-4049-a1c9-c60398b0fdce
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 683815
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.75(c)Process changes - review, evaluation and revalidation
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Other FDA inspections of Flextronics Medical Device Manufacturing(Shenzhen) Co., Ltd.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| February 3, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 17, 2013 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Flextronics Medical Device Manufacturing(Shenzhen) Co., Ltd.
- FDA Inspection 957171 - 2016-02-03
- FDA Inspection 831935 - 2013-04-17
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