# Bioseal Corporation - Inspection Records

Source: https://www.globalkeysolutions.net/companies/bioseal-corporation/e392ffcc-a9b7-47a6-a035-860c3d99eb10

> Inspection records and compliance data for Bioseal Corporation in Placentia, California. Access full analysis and detailed observations.

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## Details

- Name: Bioseal Corporation
- FEI Number: 2027062
- City: Placentia
- State: California
- Country Name: United States
- Address Line 1: 167 W Orangethorpe Ave
- Zip Code: 92870

## Related Documents

- [FDA Inspection 1026418 - Bioseal Corporation - 2017-09-21](https://www.globalkeysolutions.net/records/fda_inspections/bioseal-corporation/e9d8f90f-88dc-40ef-9af5-b0b93365641f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 21, 2017
- [FDA Inspection 1026418 - Bioseal Corporation - 2017-09-21](https://www.globalkeysolutions.net/records/fda_inspections/bioseal-corporation/503b8b43-d9ad-489d-90c8-d1d9f83898af) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 21, 2017
- [FDA Inspection 810930 - Bioseal Corporation - 2012-12-05](https://www.globalkeysolutions.net/records/fda_inspections/bioseal-corporation/cb19b45e-8151-450c-bb18-3add9f3a9147) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 5, 2012
- [FDA Inspection 810930 - Bioseal Corporation - 2012-12-05](https://www.globalkeysolutions.net/records/fda_inspections/bioseal-corporation/874ec226-cac0-41ea-bd07-bece967c4b82) — classification: No Action Indicated (NAI), source: FDA, date: December 5, 2012
- [FDA Inspection 696333 - Bioseal Corporation - 2010-10-28](https://www.globalkeysolutions.net/records/fda_inspections/bioseal-corporation/68e74f6e-56c4-4002-afca-434290cf1721) — classification: No Action Indicated (NAI), source: FDA, date: October 28, 2010
- [FDA Inspection 696333 - Bioseal Corporation - 2010-10-28](https://www.globalkeysolutions.net/records/fda_inspections/bioseal-corporation/959c9567-73bd-4640-935e-f5f17fdbb445) — classification: No Action Indicated (NAI), source: FDA, date: October 28, 2010

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