# FDA Inspection 1026172 - Zhejiang Biomet Medical Products Co. Ltd. - August 17, 2017

Source: https://www.keypedia.com/records/fda_inspections/zhejiang-biomet-medical-products-co-ltd/23760268-eabb-4dd6-8925-aa170c6914f0
Source feed: FDA_Inspections

> FDA Inspection 1026172 for Zhejiang Biomet Medical Products Co. Ltd. on August 17, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026172
- Company Name: Zhejiang Biomet Medical Products Co. Ltd.
- Inspection Date: 2017-08-17
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 913071 - 2015-01-22](https://www.keypedia.com/records/fda_inspections/zhejiang-biomet-medical-products-co-ltd/fc5cadc8-d5bc-4c11-8b91-6f371deaad22)
- [FDA Inspection 913071 - 2015-01-22](https://www.keypedia.com/records/fda_inspections/zhejiang-biomet-medical-products-co-ltd/92073971-566f-452a-b0fc-62b6accad4ac)

Company: https://www.keypedia.com/companies/zhejiang-biomet-medical-products-co-ltd/2a3dac11-2c0d-4a88-972a-15c03cc3e18d

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