# FDA Inspection 1003014 - Biomet France SARL - February 03, 2017

Source: https://www.keypedia.com/records/fda_inspections/biomet-france-sarl/ed2af5bc-927f-4273-891b-8419ab478d99
Source feed: FDA_Inspections

> FDA Inspection 1003014 for Biomet France SARL on February 03, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1003014
- Company Name: Biomet France SARL
- Inspection Date: 2017-02-03
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1003014 - 2017-02-03](https://www.keypedia.com/records/fda_inspections/biomet-france-sarl/ab522a1a-851b-4f56-a072-a55dfd7b2a6d)

Company: https://www.keypedia.com/companies/biomet-france-sarl/08bd3ef1-8ac2-4f0c-8431-8cf0c64fa30d

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