# Bioplate Inc – FDA Inspection, Jun 1, 2026

Source: https://www.keypedia.com/records/fda_inspections/bioplate-inc/5b566f6f-e5ba-43d9-80ae-ea7a3a2e3bab
Source feed: FDA_Inspections

> FDA inspection 1320108 of Bioplate Inc, June 01, 2026. Classification: Voluntary Action Indicated (VAI). 5 citations. Form 483 issued. 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1320108
- Company Name: Bioplate Inc
- Inspection Date: 2026-06-01
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- FDA Inspection 1037318 - 2017-10-25
- FDA Inspection 885905 - 2014-07-02
- [FDA Inspection 743472 - 2011-09-01](https://www.keypedia.com/records/fda_inspections/bioplate-inc/a6af21e0-6330-4f96-b030-e775e2713d2d)

## Related Officers

- [Linda Galindo](https://www.keypedia.com/people/linda-galindo/6bc29df6-192b-4d89-92ae-20cc1660d9ad)

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

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