# BioSerenity USA, Inc. – FDA Inspection, Sep 6, 2016

Source: https://www.keypedia.com/records/fda_inspections/bioserenity-usa-inc/450493f6-97df-4870-8b3d-f923984372d1
Source feed: FDA_Inspections

> FDA inspection 985197 of BioSerenity USA, Inc., September 06, 2016. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 985197
- Company Name: BioSerenity USA, Inc.
- Inspection Date: 2016-09-06
- 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 866425 - 2014-02-05](https://www.keypedia.com/records/fda_inspections/bioserenity-usa-inc/dc783bb8-3293-4557-9c14-22abeb036590)
- [FDA Inspection 633707 - 2010-01-05](https://www.keypedia.com/records/fda_inspections/bioserenity-usa-inc/fa80b4b7-0d71-4893-b425-fa314768261b)

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

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