# TIDI Products, LLC, Ontario, CA – FDA Inspections

Source: https://www.keypedia.com/companies/tidi-products-llc/b2a33c6c-ae29-4f6e-a338-f7407337394c

> Inspection records and compliance data for TIDI Products, LLC in Ontario, California. 5 FDA inspections on record, last inspected December 09, 2021.

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## Details

- Name: TIDI Products, LLC
- FEI Number: 3016004577
- Address Line 1: 2530 E Lindsay Privado Dr Ste A
- City: Ontario
- State: California
- Zip Code: 91761
- Country Name: United States
- Address: 2530 E Lindsay Privado Dr Ste A, Ontario, California 91761, United States
- Country: United States

## Related Documents

- FDA Inspection 1161536 - TIDI Products, LLC - 2021-12-09 — classification: No Action Indicated (NAI), source: FDA, date: December 9, 2021
- FDA Inspection 1161536 - TIDI Products, LLC - 2021-12-09 — classification: No Action Indicated (NAI), source: FDA, date: December 9, 2021
- [FDA Inspection 1055339 - TIDI Products, LLC - 2018-05-30](https://www.keypedia.com/records/fda_inspections/tidi-products-llc/a89b5710-367a-47be-a726-535eb8b60621) — classification: No Action Indicated (NAI), source: FDA, date: May 30, 2018
- FDA Inspection 1055339 - TIDI Products, LLC - 2018-05-30 — classification: No Action Indicated (NAI), source: FDA, date: May 30, 2018
- FDA Inspection 885452 - TIDI Products, LLC - 2014-06-25 — classification: No Action Indicated (NAI), source: FDA, date: June 25, 2014
- FDA Inspection 885452 - TIDI Products, LLC - 2014-06-25 — classification: No Action Indicated (NAI), source: FDA, date: June 25, 2014
- FDA Inspection 681404 - TIDI Products, LLC - 2010-09-15 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 15, 2010
- FDA Inspection 681404 - TIDI Products, LLC - 2010-09-15 — classification: No Action Indicated (NAI), source: FDA, date: September 15, 2010
- FDA Inspection 656041 - TIDI Products, LLC - 2010-04-06 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 6, 2010
- FDA Inspection 656041 - TIDI Products, LLC - 2010-04-06 — classification: No Action Indicated (NAI), source: FDA, date: April 6, 2010

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