FDA Inspection
STRYKER (SUZHOU) MEDICAL TECHNOLOGY CO., LTD.STRYKER (SUZHOU) MEDICAL TECHNOLOGY CO., LTD. – FDA Inspection, Aug 24, 2017
Record Details
This FDA Inspection record concerns STRYKER (SUZHOU) MEDICAL TECHNOLOGY CO., LTD., with an inspection on August 24, 2017, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- August 24, 2017
- Product Type
- Devices
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ID · 498c9423-641d-485d-8296-f89f0af48b8e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1026106
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.100(b)Documentation
- 21 CFR 820.198(e)Records of complaint investigation
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Other FDA inspections of STRYKER (SUZHOU) MEDICAL TECHNOLOGY CO., LTD.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| October 29, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for STRYKER (SUZHOU) MEDICAL TECHNOLOGY CO., LTD.
- FDA Inspection 903664 - 2014-10-29
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