# Bionica Inc. – FDA Inspection, Jun 9, 2017

Source: https://www.keypedia.com/records/fda_inspections/bionica-inc/c810ca41-5bf8-4a6e-907c-7e704a59f252
Source feed: FDA_Inspections

> FDA inspection 1013534 of Bionica Inc., June 09, 2017. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1013534
- Company Name: Bionica Inc.
- Inspection Date: 2017-06-09
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- FDA Inspection 1061626 - 2018-07-16
- FDA Inspection 901734 - 2014-10-14
- FDA Inspection 633383 - 2009-12-03

## Related Officers

- [Company Rep](https://www.keypedia.com/people/mark-e-chan/2a5a3abf-96f6-4ceb-b87d-379ed5c6f47e)

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

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