# FDA Inspection 831157 - Steritec Products Mfg. Co., Inc. - May 01, 2013

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

> FDA Inspection 831157 for Steritec Products Mfg. Co., Inc. on May 01, 2013. Classification: Voluntary Action Indicated (VAI).

---

## 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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1192098 - 2022-12-01](https://www.globalkeysolutions.net/api/records/fda_inspections/steritec-products-mfg-co-inc/b4d46909-e1e3-40f3-91eb-105fea874a65/)
- [FDA Inspection 1192098 - 2022-12-01](https://www.globalkeysolutions.net/api/records/fda_inspections/steritec-products-mfg-co-inc/40216103-6ccf-4101-86a7-fcce71f4ea27/)
- [FDA Inspection 1000027 - 2017-02-01](https://www.globalkeysolutions.net/api/records/fda_inspections/steritec-products-mfg-co-inc/3f309654-f751-497f-89bc-b61df02e5aab/)
- [FDA Inspection 831157 - 2013-05-01](https://www.globalkeysolutions.net/api/records/fda_inspections/steritec-products-mfg-co-inc/b983f302-ae0f-4cb3-93d2-3f80dcedd1a4/)
- [FDA Inspection 675641 - 2010-08-12](https://www.globalkeysolutions.net/api/records/fda_inspections/steritec-products-mfg-co-inc/170e595f-5c1c-4526-a2f2-0a24cd9974db/)

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

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