# Generations Fertility Care, Inc., Middleton, WI – FDA Inspections

Source: https://www.keypedia.com/companies/generations-fertility-care-inc/02899d98-1180-49c9-a321-f344a7fb3488

> Inspection records and compliance data for Generations Fertility Care, Inc. in Middleton, Wisconsin. 8 FDA inspections on record, last inspected June 20, 2025.

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## Details

- Name: Generations Fertility Care, Inc.
- FEI Number: 3003678886
- Address Line 1: 2365 Deming Way
- City: Middleton
- State: Wisconsin
- Zip Code: 53562
- Country Name: United States
- Address: 2365 Deming Way, Middleton, Wisconsin 53562, United States
- Country: United States

## Related Documents

- FDA Inspection 1276419 - Generations Fertility Care, Inc. - 2025-06-20 — source: FDA, date: June 20, 2025
- FDA Inspection 1276419 - Generations Fertility Care, Inc. - 2025-06-20 — classification: No Action Indicated (NAI), source: FDA, date: June 20, 2025
- FDA Inspection 1195714 - Generations Fertility Care, Inc. - 2023-01-05 — classification: No Action Indicated (NAI), source: FDA, date: January 5, 2023
- FDA Inspection 1195714 - Generations Fertility Care, Inc. - 2023-01-05 — classification: No Action Indicated (NAI), source: FDA, date: January 5, 2023
- FDA Inspection 1195714 - Generations Fertility Care, Inc. - 2023-01-05 — classification: No Action Indicated (NAI), source: FDA, date: January 5, 2023
- FDA Inspection 1061264 - Generations Fertility Care, Inc. - 2018-06-29 — classification: No Action Indicated (NAI), source: FDA, date: June 29, 2018
- FDA Inspection 1061264 - Generations Fertility Care, Inc. - 2018-06-29 — classification: No Action Indicated (NAI), source: FDA, date: June 29, 2018
- FDA Inspection 963081 - Generations Fertility Care, Inc. - 2016-03-17 — classification: No Action Indicated (NAI), source: FDA, date: March 17, 2016
- FDA Inspection 864713 - Generations Fertility Care, Inc. - 2014-01-21 — classification: No Action Indicated (NAI), source: FDA, date: January 21, 2014
- FDA Inspection 776308 - Generations Fertility Care, Inc. - 2012-04-10 — classification: No Action Indicated (NAI), source: FDA, date: April 10, 2012

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