# Bioseal – FDA Inspection, Sep 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/bioseal/e9d8f90f-88dc-40ef-9af5-b0b93365641f
Source feed: FDA_Inspections

> FDA inspection 1026418 of Bioseal, September 21, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026418
- Company Name: Bioseal
- Inspection Date: 2017-09-21
- 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: 2

## Related Documents

- FDA Inspection 810930 - 2012-12-05
- [FDA Inspection 696333 - 2010-10-28](https://www.keypedia.com/records/fda_inspections/bioseal/959c9567-73bd-4640-935e-f5f17fdbb445)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/kirtida-patel/c62852cf-9724-4296-bc4b-de8993dcf716)

Company: https://www.keypedia.com/companies/bioseal/e392ffcc-a9b7-47a6-a035-860c3d99eb10

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