# AJLS Enterprises, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/ajls-enterprises-inc/3f0c0553-0acc-4896-87f6-a645efdd5bff

> Inspection records and compliance data for AJLS Enterprises, Inc. in Madison, Wisconsin. Access full analysis and detailed observations.

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## Details

- Name: AJLS Enterprises, Inc.
- FEI Number: 2112908
- City: Madison
- State: Wisconsin
- Country Name: United States
- Address Line 1: 514 Division St
- Zip Code: 53704

## Related Documents

- [FDA Inspection 1262169 - AJLS Enterprises, Inc. - 2025-04-29](https://www.globalkeysolutions.net/records/fda_inspections/ajls-enterprises-inc/4009cd19-f079-4a4e-903e-9aec1d74a7e3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 29, 2025
- [FDA Inspection 1262169 - AJLS Enterprises, Inc. - 2025-04-29](https://www.globalkeysolutions.net/records/fda_inspections/ajls-enterprises-inc/7153eb6a-61fd-475e-afd4-9e6f471b1bc9) — classification: No Action Indicated (NAI), source: FDA, date: April 29, 2025
- [FDA Inspection 1262169 - AJLS Enterprises, Inc. - 2025-04-29](https://www.globalkeysolutions.net/records/fda_inspections/ajls-enterprises-inc/efd3b75a-1248-4935-9b1b-546803213ed4) — classification: No Action Indicated (NAI), source: FDA, date: April 29, 2025
- [FDA Inspection 993303 - AJLS Enterprises, Inc. - 2016-11-17](https://www.globalkeysolutions.net/records/fda_inspections/ajls-enterprises-inc/fbb29229-5181-4775-80f0-5e8ae4db5066) — classification: No Action Indicated (NAI), source: FDA, date: November 17, 2016
- [FDA Inspection 807214 - AJLS Enterprises, Inc. - 2012-11-13](https://www.globalkeysolutions.net/records/fda_inspections/ajls-enterprises-inc/ed958497-78e8-4bff-ae3f-0506ae1070c7) — classification: No Action Indicated (NAI), source: FDA, date: November 13, 2012
- [FDA Inspection 635975 - AJLS Enterprises, Inc. - 2009-12-30](https://www.globalkeysolutions.net/records/fda_inspections/ajls-enterprises-inc/581bd927-c09e-42a2-8801-d320dde68145) — classification: No Action Indicated (NAI), source: FDA, date: December 30, 2009

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