# Primus Sterilizer Co Inc – FDA Inspection, Feb 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/primus-sterilizer-co-inc/b8950f4d-3e48-4ff2-b0d0-f15899bc7114
Source feed: FDA_Inspections

> FDA inspection 1003248 of Primus Sterilizer Co Inc, February 21, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1003248
- Company Name: Primus Sterilizer Co Inc
- Inspection Date: 2017-02-21
- 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 1045252 - 2018-03-22](https://www.keypedia.com/records/fda_inspections/primus-sterilizer-co-inc/4cf2b354-ac85-461d-9a5e-01295fa2d8b1)
- [FDA Inspection 914385 - 2015-01-28](https://www.keypedia.com/records/fda_inspections/primus-sterilizer-co-inc/8680d09d-f99f-46d4-b3e5-d8bfa7094d79)
- FDA Inspection 861769 - 2013-12-05
- FDA Inspection 834493 - 2013-05-10
- FDA Inspection 656794 - 2010-03-26

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/eric-m-padgett/a42150bc-aa7f-4076-8a68-af47ff465bac)

Company: https://www.keypedia.com/companies/primus-sterilizer-co-inc/536405a8-3898-4455-a170-d3b0102d3fcd

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