# Primus Sterilizer Co Inc – FDA Inspection, Mar 22, 2018

Source: https://www.keypedia.com/records/fda_inspections/primus-sterilizer-co-inc/4cf2b354-ac85-461d-9a5e-01295fa2d8b1
Source feed: FDA_Inspections

> FDA inspection 1045252 of Primus Sterilizer Co Inc, March 22, 2018. Classification: Voluntary Action Indicated (VAI). 3 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: 1045252
- Company Name: Primus Sterilizer Co Inc
- Inspection Date: 2018-03-22
- 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: 3

## Related Documents

- [FDA Inspection 1003248 - 2017-02-21](https://www.keypedia.com/records/fda_inspections/primus-sterilizer-co-inc/b8950f4d-3e48-4ff2-b0d0-f15899bc7114)
- [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

- [Investigator](https://www.keypedia.com/people/eric-c-fox/218af117-1551-476f-80ba-172e2cd6baee)

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