FDA Inspection
Anhui Kangda Medical Products Co., Ltd.Anhui Kangda Medical Products Co., Ltd. – FDA Inspection, Jun 13, 2018
Record Details
This FDA Inspection record concerns Anhui Kangda Medical Products Co., Ltd., with an inspection on June 13, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · c1059927-328a-4dd3-962d-f0d54daa56a1
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1056979
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Anhui Kangda Medical Products Co., Ltd.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| November 20, 2014 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| November 19, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Anhui Kangda Medical Products Co., Ltd.
- FDA Inspection 907776 - 2014-11-20
- FDA Inspection 907781 - 2014-11-19
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