# Animart, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/animart-inc/cfb20acc-619b-410c-b201-a926584454a9

> Inspection records and compliance data for Animart, Inc. in Beaver Dam, Wisconsin. Access full analysis and detailed observations.

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## Details

- Name: Animart, Inc.
- FEI Number: 2129513
- City: Beaver Dam
- State: Wisconsin
- Country Name: United States
- Address Line 1: 1240 Green Valley Rd
- Zip Code: 53916

## Related Documents

- [FDA Inspection 1267707 - Animart, Inc. - 2025-04-17](https://www.keypedia.com/records/fda_inspections/animart-inc/6efe4633-0f50-4781-882c-fe125f3c1f4b) — source: FDA, date: April 17, 2025
- [FDA Inspection 1231724 - Animart, Inc. - 2024-02-15](https://www.keypedia.com/records/fda_inspections/animart-inc/c87a9479-894d-4dff-8bcb-2346f67632c6) — classification: No Action Indicated (NAI), source: FDA, date: February 15, 2024
- [FDA Inspection 1227717 - Animart, Inc. - 2024-01-19](https://www.keypedia.com/records/fda_inspections/animart-inc/ba3c74c1-c718-44eb-82d8-a4e832a4440d) — classification: No Action Indicated (NAI), source: FDA, date: January 19, 2024
- [FDA Inspection 1223917 - Animart, Inc. - 2023-11-07](https://www.keypedia.com/records/fda_inspections/animart-inc/163f91fc-5aa5-41a7-bf16-953999067fa7) — classification: No Action Indicated (NAI), source: FDA, date: November 7, 2023
- [FDA Inspection 1223873 - Animart, Inc. - 2023-10-30](https://www.keypedia.com/records/fda_inspections/animart-inc/8591419d-21d7-46c7-9144-d9f48233eaee) — classification: No Action Indicated (NAI), source: FDA, date: October 30, 2023
- [FDA Inspection 1220615 - Animart, Inc. - 2023-10-17](https://www.keypedia.com/records/fda_inspections/animart-inc/73d3aaa9-6fdd-488b-a50e-1b17e1850999) — classification: No Action Indicated (NAI), source: FDA, date: October 17, 2023
- [FDA Inspection 1205577 - Animart, Inc. - 2023-05-10](https://www.keypedia.com/records/fda_inspections/animart-inc/632952f9-a727-43f1-95ea-eca2e32d15a5) — classification: No Action Indicated (NAI), source: FDA, date: May 10, 2023
- [FDA Inspection 1121780 - Animart, Inc. - 2020-01-31](https://www.keypedia.com/records/fda_inspections/animart-inc/7f01b305-92e1-49d6-a607-d070f288a235) — classification: No Action Indicated (NAI), source: FDA, date: January 31, 2020
- [FDA Inspection 1082702 - Animart, Inc. - 2019-03-12](https://www.keypedia.com/records/fda_inspections/animart-inc/f0ee1cb1-8a63-455c-b4d4-758871b74af7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 12, 2019
- [FDA Inspection 1071522 - Animart, Inc. - 2018-11-13](https://www.keypedia.com/records/fda_inspections/animart-inc/329b2e67-0cf4-4174-a819-32f69f4c0019) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 13, 2018

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