# FDA Inspection 848712 - ORICH MEDICAL EQUIPMENT (TIANJIN) CO., LTD - August 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 for ORICH MEDICAL EQUIPMENT (TIANJIN) CO., LTD on August 15, 2013. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 848712 - 2013-08-15](https://www.keypedia.com/records/fda_inspections/orich-medical-equipment-tianjin-co-ltd/69e24155-a79b-4614-a261-83671002fb17)

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