FDA Inspection
ORICH MEDICAL EQUIPMENT (TIANJIN) CO., LTDORICH MEDICAL EQUIPMENT (TIANJIN) CO., LTD – FDA Inspection, Aug 15, 2013
Record Details
This FDA Inspection record concerns ORICH MEDICAL EQUIPMENT (TIANJIN) CO., LTD, with an inspection on August 15, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- August 15, 2013
- Product Type
- Devices
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ID · c912c01d-d9df-4ef1-9ea1-cb0bccfb73a0
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 848712
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of ORICH MEDICAL EQUIPMENT (TIANJIN) CO., LTD
1| Date | Classification | Office | Project area |
|---|---|---|---|
| February 24, 2017 | Not classified | Office of Inspections and Investigations |
Other documents for ORICH MEDICAL EQUIPMENT (TIANJIN) CO., LTD
- FDA Inspection 1010182 - 2017-02-24
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