# FDA Inspection 1117375 - Bionik, Inc. - February 10, 2020

Source: https://www.keypedia.com/records/fda_inspections/bionik-inc/473defcd-e0fa-4fe4-997d-39bc955130b0
Source feed: FDA_Inspections

> FDA Inspection 1117375 for Bionik, Inc. on February 10, 2020. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1117375
- Company Name: Bionik, Inc.
- Inspection Date: 2020-02-10
- 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 1117375 - 2020-02-10](https://www.keypedia.com/records/fda_inspections/bionik-inc/3acd662c-3fa7-4d28-91f3-5940e4d0b125)
- [FDA Inspection 945197 - 2015-09-10](https://www.keypedia.com/records/fda_inspections/bionik-inc/27abc5a7-6eda-4250-8c58-2200e7bda472)
- [FDA Inspection 775687 - 2012-04-03](https://www.keypedia.com/records/fda_inspections/bionik-inc/e8bffc8a-8b2d-4ad9-ad7e-6bd95e21be09)

Company: https://www.keypedia.com/companies/bionik-inc/ffa246f2-6f42-424a-bd98-18179f15e0ba

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