# Steritec Products Mfg. Co., Inc. - Inspection Records

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

> Inspection records and compliance data for Steritec Products Mfg. Co., Inc. in Englewood, Colorado. Access full analysis and detailed observations.

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## Details

- Name: Steritec Products Mfg. Co., Inc.
- FEI Number: 1000125215
- City: Englewood
- State: Colorado
- Country Name: United States
- Address Line 1: 74 Inverness Dr E
- Zip Code: 80112

## Related Documents

- [483 - Steritec Products Mfg. Co., Inc. - 2022-12-01](https://www.globalkeysolutions.net/records/483/steritec-products-mfg-co-inc/ff2a2d4f-d21b-4b4d-87fc-e82473215bca) — source: FDA, date: December 1, 2022
- [FDA Inspection 1192098 - Steritec Products Mfg. Co., Inc. - 2022-12-01](https://www.globalkeysolutions.net/records/fda_inspections/steritec-products-mfg-co-inc/b4d46909-e1e3-40f3-91eb-105fea874a65) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 1, 2022
- [FDA Inspection 1192098 - Steritec Products Mfg. Co., Inc. - 2022-12-01](https://www.globalkeysolutions.net/records/fda_inspections/steritec-products-mfg-co-inc/40216103-6ccf-4101-86a7-fcce71f4ea27) — classification: No Action Indicated (NAI), source: FDA, date: December 1, 2022
- [FDA Inspection 1000027 - Steritec Products Mfg. Co., Inc. - 2017-02-01](https://www.globalkeysolutions.net/records/fda_inspections/steritec-products-mfg-co-inc/3f309654-f751-497f-89bc-b61df02e5aab) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 1, 2017
- [FDA Inspection 831157 - Steritec Products Mfg. Co., Inc. - 2013-05-01](https://www.globalkeysolutions.net/records/fda_inspections/steritec-products-mfg-co-inc/fa054a24-804c-4708-8b8e-8b1c5e809ef7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 1, 2013
- [FDA Inspection 831157 - Steritec Products Mfg. Co., Inc. - 2013-05-01](https://www.globalkeysolutions.net/records/fda_inspections/steritec-products-mfg-co-inc/b983f302-ae0f-4cb3-93d2-3f80dcedd1a4) — classification: No Action Indicated (NAI), source: FDA, date: May 1, 2013
- [FDA Inspection 675641 - Steritec Products Mfg. Co., Inc. - 2010-08-12](https://www.globalkeysolutions.net/records/fda_inspections/steritec-products-mfg-co-inc/170e595f-5c1c-4526-a2f2-0a24cd9974db) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 12, 2010
- [FDA Inspection 675641 - Steritec Products Mfg. Co., Inc. - 2010-08-12](https://www.globalkeysolutions.net/records/fda_inspections/steritec-products-mfg-co-inc/1d170122-357b-4f44-ba2d-ff132ae18cf7) — classification: No Action Indicated (NAI), source: FDA, date: August 12, 2010
- [FDA Inspection 585881 - Steritec Products Mfg. Co., Inc. - 2009-06-02](https://www.globalkeysolutions.net/records/fda_inspections/steritec-products-mfg-co-inc/11ef6a7c-7584-4983-a204-2989923398b6) — classification: Official Action Indicated (OAI), source: FDA, date: June 2, 2009
- [FDA Inspection 585881 - Steritec Products Mfg. Co., Inc. - 2009-06-02](https://www.globalkeysolutions.net/records/fda_inspections/steritec-products-mfg-co-inc/622c8be2-066c-4407-b695-8c2c349cc779) — classification: No Action Indicated (NAI), source: FDA, date: June 2, 2009

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