# FDA Inspection 900813 - Ningbo Caremed Medical Products Co. Ltd. - July 10, 2014

Source: https://www.keypedia.com/records/fda_inspections/ningbo-caremed-medical-products-co-ltd/1ee94097-e119-411e-bfb7-3151936d184b
Source feed: FDA_Inspections

> FDA Inspection 900813 for Ningbo Caremed Medical Products Co. Ltd. on July 10, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 900813
- Company Name: Ningbo Caremed Medical Products Co. Ltd.
- Inspection Date: 2014-07-10
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 993755 - 2016-11-03](https://www.keypedia.com/records/fda_inspections/ningbo-caremed-medical-products-co-ltd/880d14cc-a146-4996-9521-6de98044072e)

Company: https://www.keypedia.com/companies/ningbo-caremed-medical-products-co-ltd/53dab110-1d57-4f71-89c5-b07a06ba132d

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