# ReproTech, Ltd., Saint Paul, MN – FDA Inspections

Source: https://www.keypedia.com/companies/reprotech-ltd/3e4f70ef-eb22-4290-a97f-06fe0b9a7b87

> Inspection records and compliance data for ReproTech, Ltd. in Saint Paul, Minnesota. 6 FDA inspections on record, last inspected January 23, 2020.

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## Details

- Name: ReproTech, Ltd.
- FEI Number: 3003651454
- Address Line 1: 33 5th Ave NW Ste 900
- City: Saint Paul
- State: Minnesota
- Zip Code: 55112
- Country Name: United States
- Address: 33 5th Ave NW Ste 900, Saint Paul, Minnesota 55112, United States
- Country: United States

## Related Documents

- FDA Inspection 1116523 - ReproTech, Ltd. - 2020-01-23 — classification: No Action Indicated (NAI), source: FDA, date: January 23, 2020
- FDA Inspection 1116523 - ReproTech, Ltd. - 2020-01-23 — classification: No Action Indicated (NAI), source: FDA, date: January 23, 2020
- FDA Inspection 1037727 - ReproTech, Ltd. - 2018-01-04 — classification: No Action Indicated (NAI), source: FDA, date: January 4, 2018
- FDA Inspection 1037727 - ReproTech, Ltd. - 2018-01-04 — classification: No Action Indicated (NAI), source: FDA, date: January 4, 2018
- [FDA Inspection 952457 - ReproTech, Ltd. - 2015-12-15](https://www.keypedia.com/records/fda_inspections/reprotech-ltd/793908df-4601-4cf8-adb1-57e361d5a729) — classification: No Action Indicated (NAI), source: FDA, date: December 15, 2015
- FDA Inspection 863862 - ReproTech, Ltd. - 2014-01-29 — classification: No Action Indicated (NAI), source: FDA, date: January 29, 2014
- FDA Inspection 767137 - ReproTech, Ltd. - 2012-02-08 — classification: No Action Indicated (NAI), source: FDA, date: February 8, 2012
- FDA Inspection 637647 - ReproTech, Ltd. - 2010-01-08 — classification: No Action Indicated (NAI), source: FDA, date: January 8, 2010

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