# FDA Inspection 1057663 - MicroPort Orthopedics Inc. - June 29, 2018

Source: https://www.keypedia.com/records/fda_inspections/microport-orthopedics-inc/72477909-75ec-4729-8777-e7b67b86d5d6
Source feed: FDA_Inspections

> FDA Inspection 1057663 for MicroPort Orthopedics Inc. on June 29, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1057663
- Company Name: MicroPort Orthopedics Inc.
- Inspection Date: 2018-06-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1198299 - 2023-02-08](https://www.keypedia.com/records/fda_inspections/microport-orthopedics-inc/59860ff4-fd21-4de9-b66b-20b45497ee17)
- [FDA Inspection 937709 - 2015-08-19](https://www.keypedia.com/records/fda_inspections/microport-orthopedics-inc/ca4d9728-cf77-4314-a741-2bf2028fe50c)
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Company: https://www.keypedia.com/companies/microport-orthopedics-inc/dfec990c-1211-40dc-8ee3-0874e9d539a5

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