# FDA Inspection 633707 - BioSerenity USA, Inc. - January 05, 2010

Source: https://www.globalkeysolutions.net/records/fda_inspections/bioserenity-usa-inc/fa80b4b7-0d71-4893-b425-fa314768261b/
Source feed: FDA_Inspections

> FDA Inspection 633707 for BioSerenity USA, Inc. on January 05, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 633707
- Company Name: BioSerenity USA, Inc.
- Inspection Date: 2010-01-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/bioserenity-usa-inc/a9bff44c-c77e-4300-9270-6705c839e164

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