# Amerilab Technologies, Inc, Plymouth, MN – FDA Inspections

Source: https://www.keypedia.com/companies/amerilab-technologies-inc/c39c8583-cc97-4e61-8caa-99e8fef9cbd9

> Inspection records and compliance data for Amerilab Technologies, Inc in Plymouth, Minnesota. 10 FDA inspections on record (1 OAI), last inspected March 14, 2024.

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## Details

- Name: Amerilab Technologies, Inc
- FEI Number: 3000206080
- Address Line 1: 2765 Niagara Ln N
- City: Plymouth
- State: Minnesota
- Zip Code: 55447
- Country Name: United States
- Address: 2765 Niagara Ln N, Plymouth, Minnesota 55447, United States
- Country: United States

## Related Documents

- FDA Inspection 1235570 - Amerilab Technologies, Inc - 2024-03-14 — classification: No Action Indicated (NAI), source: FDA, date: March 14, 2024
- FDA Inspection 1235570 - Amerilab Technologies, Inc - 2024-03-14 — classification: No Action Indicated (NAI), source: FDA, date: March 14, 2024
- FDA Inspection 1149887 - Amerilab Technologies, Inc - 2021-08-18 — classification: No Action Indicated (NAI), source: FDA, date: August 18, 2021
- FDA Inspection 1011653 - Amerilab Technologies, Inc - 2017-04-17 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 17, 2017
- FDA Inspection 1011653 - Amerilab Technologies, Inc - 2017-04-17 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 17, 2017
- FDA Inspection 871240 - Amerilab Technologies, Inc - 2014-03-20 — classification: No Action Indicated (NAI), source: FDA, date: March 20, 2014
- FDA Inspection 871240 - Amerilab Technologies, Inc - 2014-03-20 — classification: No Action Indicated (NAI), source: FDA, date: March 20, 2014
- FDA Inspection 870733 - Amerilab Technologies, Inc - 2014-03-20 — classification: No Action Indicated (NAI), source: FDA, date: March 20, 2014
- FDA Inspection 778185 - Amerilab Technologies, Inc - 2012-04-23 — classification: No Action Indicated (NAI), source: FDA, date: April 23, 2012
- FDA Inspection 778374 - Amerilab Technologies, Inc - 2012-04-23 — classification: No Action Indicated (NAI), source: FDA, date: April 23, 2012

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