# ReproTech, Ltd. - Inspection Records

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. Access full analysis and detailed observations.

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## Details

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

## Related Documents

- [FDA Inspection 1116523 - ReproTech, Ltd. - 2020-01-23](https://www.keypedia.com/records/fda_inspections/reprotech-ltd/0eacaa40-5161-496c-a763-aefd763b3381) — classification: No Action Indicated (NAI), source: FDA, date: January 23, 2020
- [FDA Inspection 1116523 - ReproTech, Ltd. - 2020-01-23](https://www.keypedia.com/records/fda_inspections/reprotech-ltd/d8d66625-1f97-4207-977b-5f927b3fe346) — classification: No Action Indicated (NAI), source: FDA, date: January 23, 2020
- [FDA Inspection 1037727 - ReproTech, Ltd. - 2018-01-04](https://www.keypedia.com/records/fda_inspections/reprotech-ltd/73c8a975-a572-45da-92da-592ad75bce1d) — classification: No Action Indicated (NAI), source: FDA, date: January 4, 2018
- [FDA Inspection 1037727 - ReproTech, Ltd. - 2018-01-04](https://www.keypedia.com/records/fda_inspections/reprotech-ltd/7bb5f49c-4bc9-47dc-bcba-bb1c904c1a2b) — 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](https://www.keypedia.com/records/fda_inspections/reprotech-ltd/4623c23f-c74b-4530-aba3-174810dc5249) — classification: No Action Indicated (NAI), source: FDA, date: January 29, 2014
- [FDA Inspection 767137 - ReproTech, Ltd. - 2012-02-08](https://www.keypedia.com/records/fda_inspections/reprotech-ltd/bed94aee-66bd-45ad-a7f7-440fe7c96c17) — classification: No Action Indicated (NAI), source: FDA, date: February 8, 2012
- [FDA Inspection 637647 - ReproTech, Ltd. - 2010-01-08](https://www.keypedia.com/records/fda_inspections/reprotech-ltd/9f1822d7-f437-4e2f-8a18-0a11ee4f3632) — classification: No Action Indicated (NAI), source: FDA, date: January 8, 2010

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