# FDA Inspection 858168 - PerioSeal, Inc. - December 11, 2013

Source: https://www.keypedia.com/records/fda_inspections/perioseal-inc/12b634b6-e510-427a-b6dc-fc3308b5a25a
Source feed: FDA_Inspections

> FDA Inspection 858168 for PerioSeal, Inc. on December 11, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 858168
- Company Name: PerioSeal, Inc.
- Inspection Date: 2013-12-11
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 794886 - 2012-08-09](https://www.keypedia.com/records/fda_inspections/perioseal-inc/15f019fb-f0eb-4fb3-9b71-600b41a917b9)
- [FDA Inspection 794886 - 2012-08-09](https://www.keypedia.com/records/fda_inspections/perioseal-inc/eed3b792-408a-4045-bb5f-e225c0891569)

Company: https://www.keypedia.com/companies/perioseal-inc/ec9bfe37-ad1d-45dc-8a54-f6b731ee2b24

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