# ORICH MEDICAL EQUIPMENT (TIANJIN) CO., LTD – FDA Inspection, Aug 15, 2013

Source: https://www.keypedia.com/records/fda_inspections/orich-medical-equipment-tianjin-co-ltd/c912c01d-d9df-4ef1-9ea1-cb0bccfb73a0
Source feed: FDA_Inspections

> FDA inspection 848712 of ORICH MEDICAL EQUIPMENT (TIANJIN) CO., LTD, August 15, 2013. Classification: Voluntary Action Indicated (VAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 848712
- Company Name: ORICH MEDICAL EQUIPMENT (TIANJIN) CO., LTD
- Inspection Date: 2013-08-15
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1010182 - 2017-02-24

Company: https://www.keypedia.com/companies/orich-medical-equipment-tianjin-co-ltd/964b46c0-11b0-4c87-9388-5c3be404b96c

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7