# Sterimed, LLC – FDA Inspection, Nov 6, 2013

Source: https://www.keypedia.com/records/fda_inspections/sterimed-llc/c96ce0d2-09fe-490c-93a8-e81f3cec2b0b
Source feed: FDA_Inspections

> FDA inspection 855408 of Sterimed, LLC, November 06, 2013. Classification: Voluntary Action Indicated (VAI). 4 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: 855408
- Company Name: Sterimed, LLC
- Inspection Date: 2013-11-06
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 1006535 - 2017-03-20](https://www.keypedia.com/records/fda_inspections/sterimed-llc/cbcc3842-56d4-46c0-b395-b4193b58055f)
- FDA Inspection 716528 - 2011-03-14

Company: https://www.keypedia.com/companies/sterimed-llc/3dd21946-c5a2-48eb-ba8a-782430e85ac3

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