# Steritec Products Mfg. Co., Inc. – FDA Inspection, May 1, 2013

Source: https://www.keypedia.com/records/fda_inspections/steritec-products-mfg-co-inc/fa054a24-804c-4708-8b8e-8b1c5e809ef7
Source feed: FDA_Inspections

> FDA inspection 831157 of Steritec Products Mfg. Co., Inc., May 01, 2013. Classification: Voluntary Action Indicated (VAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 831157
- Company Name: Steritec Products Mfg. Co., Inc.
- Inspection Date: 2013-05-01
- 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: 0

## Related Documents

- FDA Inspection 1192098 - 2022-12-01
- [FDA Inspection 1000027 - 2017-02-01](https://www.keypedia.com/records/fda_inspections/steritec-products-mfg-co-inc/3f309654-f751-497f-89bc-b61df02e5aab)
- [FDA Inspection 675641 - 2010-08-12](https://www.keypedia.com/records/fda_inspections/steritec-products-mfg-co-inc/1d170122-357b-4f44-ba2d-ff132ae18cf7)
- [FDA Inspection 585881 - 2009-06-02](https://www.keypedia.com/records/fda_inspections/steritec-products-mfg-co-inc/11ef6a7c-7584-4983-a204-2989923398b6)

Company: https://www.keypedia.com/companies/steritec-products-mfg-co-inc/5c4ae5a4-e14a-4059-9ffd-85b7697464c8

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