# FDA Inspection 1037318 - Bioplate Inc - October 25, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/bioplate-inc/90fe6c71-b5cd-4d70-9d21-722bf4e9657e
Source feed: FDA_Inspections

> FDA Inspection 1037318 for Bioplate Inc on October 25, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1037318
- Company Name: Bioplate Inc
- Inspection Date: 2017-10-25
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 885905 - 2014-07-02](https://www.globalkeysolutions.net/records/fda_inspections/bioplate-inc/5e59495a-0309-4ab5-bbc4-8fb85614944d)
- [FDA Inspection 885905 - 2014-07-02](https://www.globalkeysolutions.net/records/fda_inspections/bioplate-inc/5d96c0e9-be59-440f-abc8-12859831db6e)
- [FDA Inspection 743472 - 2011-09-01](https://www.globalkeysolutions.net/records/fda_inspections/bioplate-inc/a6af21e0-6330-4f96-b030-e775e2713d2d)
- [FDA Inspection 743472 - 2011-09-01](https://www.globalkeysolutions.net/records/fda_inspections/bioplate-inc/9e5c13fe-318e-4224-8361-c223b7b7b6d7)

Company: https://www.globalkeysolutions.net/companies/bioplate-inc/e72bec43-f32d-43a9-9428-7be11cbe2e82

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