# FDA Inspection 1122266 - Bionime Usa Corp - February 25, 2020

Source: https://www.keypedia.com/records/fda_inspections/bionime-usa-corp/6e6c72c7-6d1e-4eec-8bb5-d2192aaed457
Source feed: FDA_Inspections

> FDA Inspection 1122266 for Bionime Usa Corp on February 25, 2020. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1122266
- Company Name: Bionime Usa Corp
- Inspection Date: 2020-02-25
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1122266 - 2020-02-25](https://www.keypedia.com/records/fda_inspections/bionime-usa-corp/aef92846-7d74-45d8-bd48-7703768b7449)
- [FDA Inspection 879324 - 2014-05-06](https://www.keypedia.com/records/fda_inspections/bionime-usa-corp/c855f0af-b156-415f-8bc2-ce5ea0b4bbd1)
- [FDA Inspection 879324 - 2014-05-06](https://www.keypedia.com/records/fda_inspections/bionime-usa-corp/9183c54c-4340-4230-9f8c-fee31ced02af)

Company: https://www.keypedia.com/companies/bionime-usa-corp/83f016f9-377f-4298-b157-5dde033f649f

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