# FDA Inspection 1061626 - Bionica Inc. - July 16, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/bionica-inc/1e4794bf-3c5d-4ce1-80f9-f584b60eadc5
Source feed: FDA_Inspections

> FDA Inspection 1061626 for Bionica Inc. on July 16, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1061626
- Company Name: Bionica Inc.
- Inspection Date: 2018-07-16
- 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 1061626 - 2018-07-16](https://www.globalkeysolutions.net/records/fda_inspections/bionica-inc/224fb048-30ee-4f2c-bc6f-8078e8141c7e)
- [FDA Inspection 1013534 - 2017-06-09](https://www.globalkeysolutions.net/records/fda_inspections/bionica-inc/c810ca41-5bf8-4a6e-907c-7e704a59f252)
- [FDA Inspection 1013534 - 2017-06-09](https://www.globalkeysolutions.net/records/fda_inspections/bionica-inc/c5fff3e6-ccb7-4881-9a68-d1b3619ef2b1)
- [FDA Inspection 901734 - 2014-10-14](https://www.globalkeysolutions.net/records/fda_inspections/bionica-inc/830e5b9d-5362-42dd-a941-f16d6a832851)
- [FDA Inspection 901734 - 2014-10-14](https://www.globalkeysolutions.net/records/fda_inspections/bionica-inc/c92b1b39-f58e-495f-a504-e5ff481abe8b)

Company: https://www.globalkeysolutions.net/companies/bionica-inc/8f9baba5-e23e-44c8-bce4-ffa0713be196

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