# Bioserv Corporation – FDA Inspection, Jul 31, 2017

Source: https://www.keypedia.com/records/fda_inspections/bioserv-corporation/cc62ac96-b17a-4005-bd7c-fa7981de2d9c
Source feed: FDA_Inspections

> FDA inspection 1022355 of Bioserv Corporation, July 31, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1022355
- Company Name: Bioserv Corporation
- Inspection Date: 2017-07-31
- 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: 0

## Related Documents

- FDA Inspection 1195989 - 2023-01-12
- FDA Inspection 863803 - 2014-01-23
- FDA Inspection 804269 - 2012-10-24
- [FDA Inspection 756094 - 2011-12-07](https://www.keypedia.com/records/fda_inspections/bioserv-corporation/cf5d3bc2-11f0-4560-b97c-d452d20f93b5)
- FDA Inspection 656899 - 2010-04-12

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/scott-k-zika/7f967edd-5151-438b-a0e7-dd1db8a227d1)

Company: https://www.keypedia.com/companies/bioserv-corporation/1d9b6bef-b61b-40ae-8d76-978a820dd6dc

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