# PureTek Corporation - Inspection Records

Source: https://www.keypedia.com/companies/puretek-corporation/428846ad-3d0d-4e9e-9b5e-41321940234c

> Inspection records and compliance data for PureTek Corporation in San Fernando, California. Access full analysis and detailed observations.

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## Details

- Name: PureTek Corporation
- FEI Number: 1000125324
- City: San Fernando
- State: California
- Country Name: United States
- Address Line 1: 1145 Arroyo St Ste D
- Zip Code: 91340
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, IN VITRO BIOEQUIVALENCE OR BIOANALYTICAL TESTING, PACK, REPACK

## Related Documents

- [483 - PureTek Corporation - 2025-03-07](https://www.keypedia.com/records/483/puretek-corporation/9d4c89d7-2ea2-4e56-accd-6b608d97051a) — source: FDA, date: March 7, 2025
- [FDA Inspection 1262436 - PureTek Corporation - 2025-03-07](https://www.keypedia.com/records/fda_inspections/puretek-corporation/24ebf089-ae01-4668-a6fd-05bdc2dda206) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 7, 2025
- [FDA Inspection 1116761 - PureTek Corporation - 2020-01-30](https://www.keypedia.com/records/fda_inspections/puretek-corporation/6bfc016f-d6d9-4703-b6b3-519218c7507f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 30, 2020
- [FDA Inspection 1034952 - PureTek Corporation - 2017-12-15](https://www.keypedia.com/records/fda_inspections/puretek-corporation/8f390d5c-07c0-4bc1-adcf-f3590025d6cf) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 15, 2017
- [FDA Inspection 949735 - PureTek Corporation - 2015-10-27](https://www.keypedia.com/records/fda_inspections/puretek-corporation/dce2ae31-103c-4099-a175-54f14fc3fca6) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 27, 2015
- [FDA Inspection 949735 - PureTek Corporation - 2015-10-27](https://www.keypedia.com/records/fda_inspections/puretek-corporation/37910b48-e579-4750-bd5a-4193c56e45a7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 27, 2015
- [FDA Inspection 919565 - PureTek Corporation - 2015-03-18](https://www.keypedia.com/records/fda_inspections/puretek-corporation/1844d683-1d10-4297-ba87-527f1a1f940a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 18, 2015
- [FDA Inspection 919565 - PureTek Corporation - 2015-03-18](https://www.keypedia.com/records/fda_inspections/puretek-corporation/27bb1542-f95e-475f-a0c6-00e3a54655d5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 18, 2015
- [FDA Inspection 860979 - PureTek Corporation - 2013-12-18](https://www.keypedia.com/records/fda_inspections/puretek-corporation/a8442159-0b2b-4cf1-ae07-ab0234cddc91) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 18, 2013
- [FDA Inspection 808589 - PureTek Corporation - 2012-12-04](https://www.keypedia.com/records/fda_inspections/puretek-corporation/d92797e4-3e83-44da-b9f6-92bce7662ded) — classification: No Action Indicated (NAI), source: FDA, date: December 4, 2012
- [FDA Inspection 808589 - PureTek Corporation - 2012-12-04](https://www.keypedia.com/records/fda_inspections/puretek-corporation/a719f5c6-4e22-48f0-a9ef-507acbe2e706) — classification: No Action Indicated (NAI), source: FDA, date: December 4, 2012

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## Related Officers

- [Consumer Safety Officer (Inspector)](https://www.keypedia.com/people/christopher-r-czajka/42defbf3-ea06-4090-8d51-7da2b07d9e84)
- [Lena Nguyen](https://www.keypedia.com/people/lena-nguyen/99d85719-61c2-40bb-8358-0f3a98747e0d)