# FDA Inspection 817958 - STERITECH, INC. - December 20, 2012

Source: https://www.keypedia.com/records/fda_inspections/steritech-inc/b4bfdfac-df1e-41c4-9655-bd86f321bb71
Source feed: FDA_Inspections

> FDA Inspection 817958 for STERITECH, INC. on December 20, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 817958
- Company Name: STERITECH, INC.
- Inspection Date: 2012-12-20
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/steritech-inc/d82fe0a3-7c69-46ed-82ff-4a3beef4eab9

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