# SteriGear, LLC – FDA Inspection, Mar 22, 2023

Source: https://www.keypedia.com/records/fda_inspections/sterigear-llc/a819ffee-07fc-402b-9570-f43b6ad412b6
Source feed: FDA_Inspections

> FDA inspection 1200541 of SteriGear, LLC, March 22, 2023. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1200541
- Company Name: SteriGear, LLC
- Inspection Date: 2023-03-22
- 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: 2

## Related Documents

- FDA Inspection 1004659 - 2017-03-06
- [FDA Inspection 878262 - 2014-05-09](https://www.keypedia.com/records/fda_inspections/sterigear-llc/2f6e6f99-a566-4f53-9bc7-5d7fee722ca9)
- [FDA Inspection 714471 - 2011-03-17](https://www.keypedia.com/records/fda_inspections/sterigear-llc/ebc8b275-d57b-47bf-942d-1418b6fad3c2)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/james-r-montero/ce2d19fd-25b7-423e-9132-5d6f582380d2)

Company: https://www.keypedia.com/companies/sterigear-llc/6fc23f03-ccbf-4165-837b-b72883012630

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