# Mirrotek International, LLC - Inspection Records

Source: https://www.globalkeysolutions.net/companies/mirrotek-international-llc/e983ab52-7101-4606-b50d-8dff769c70fa

> Inspection records and compliance data for Mirrotek International, LLC in Passaic, New Jersey. Access full analysis and detailed observations.

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## Details

- Name: Mirrotek International, LLC
- FEI Number: 3004448310
- City: Passaic
- State: New Jersey
- Country Name: United States
- Address Line 1: 90 Dayton Ave Ste 22 Ste 1f
- Zip Code: 07055

## Related Documents

- [FDA Inspection 1128852 - Mirrotek International, LLC - 2020-08-26](https://www.globalkeysolutions.net/records/fda_inspections/mirrotek-international-llc/35a6d9e3-5eb7-4487-9c5f-8cbe8afca78b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 26, 2020
- [FDA Inspection 1059385 - Mirrotek International, LLC - 2018-06-19](https://www.globalkeysolutions.net/records/fda_inspections/mirrotek-international-llc/283ebf1f-c974-4c0d-bb8a-67e5f7f6040f) — classification: No Action Indicated (NAI), source: FDA, date: June 19, 2018
- [FDA Inspection 942392 - Mirrotek International, LLC - 2015-09-17](https://www.globalkeysolutions.net/records/fda_inspections/mirrotek-international-llc/d8068522-9d9d-4194-8f01-565e5b76a0df) — classification: No Action Indicated (NAI), source: FDA, date: September 17, 2015
- [FDA Inspection 787882 - Mirrotek International, LLC - 2012-06-20](https://www.globalkeysolutions.net/records/fda_inspections/mirrotek-international-llc/e46a0724-9ccb-4892-8bda-b97c75ae2af9) — classification: No Action Indicated (NAI), source: FDA, date: June 20, 2012
- [WARNING_LETTER - Mirrotek International, LLC - 2011-09-30](https://www.globalkeysolutions.net/records/warning_letter/mirrotek-international-llc/6d20b107-16c8-4842-85f6-fabfe2889bd0) — source: FDA, date: September 30, 2011
- [FDA Inspection 747101 - Mirrotek International, LLC - 2011-09-30](https://www.globalkeysolutions.net/records/fda_inspections/mirrotek-international-llc/2b933cc5-0ad4-4817-a747-47a59e5bdf8b) — classification: Official Action Indicated (OAI), source: FDA, date: September 30, 2011

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