# Welmed Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/welmed-inc/778f4417-f6f6-466b-97e7-3cde8e60ac5b

> Inspection records and compliance data for Welmed Inc. in Chicago, Illinois. Access full analysis and detailed observations.

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## Details

- Name: Welmed Inc.
- FEI Number: 3005841027
- City: Chicago
- State: Illinois
- Country Name: United States
- Address Line 1: 401 N Michigan Ave Ste 1200
- Zip Code: 60611

## Related Documents

- [FDA Inspection 1303608 - Welmed Inc. - 2026-02-19](https://www.globalkeysolutions.net/records/fda_inspections/welmed-inc/fb929d29-e3a6-4ac2-96e2-f71f05fddbc4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 19, 2026
- [FDA Inspection 1303608 - Welmed Inc. - 2026-02-19](https://www.globalkeysolutions.net/records/fda_inspections/welmed-inc/62f1f959-2e7c-44d2-b00e-a2f85901c5ae) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 19, 2026
- [483 - Welmed Inc. - 2022-03-23](https://www.globalkeysolutions.net/records/483/welmed-inc/f7fed4af-0536-4d7a-a0e3-09c98a3fc5a2) — source: FDA, date: March 23, 2022
- [FDA Inspection 1165199 - Welmed Inc. - 2022-03-23](https://www.globalkeysolutions.net/records/fda_inspections/welmed-inc/233b9a21-b5b8-48ae-94de-aa02058ee7ca) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 23, 2022
- [FDA Inspection 1165199 - Welmed Inc. - 2022-03-23](https://www.globalkeysolutions.net/records/fda_inspections/welmed-inc/6f2f1571-fbec-4cf7-ad79-c3b1c9c15564) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 23, 2022
- [FDA Inspection 1026884 - Welmed Inc. - 2017-08-30](https://www.globalkeysolutions.net/records/fda_inspections/welmed-inc/41364eae-92f4-41c5-8655-d8c6f1abb31a) — classification: No Action Indicated (NAI), source: FDA, date: August 30, 2017
- [FDA Inspection 1026884 - Welmed Inc. - 2017-08-30](https://www.globalkeysolutions.net/records/fda_inspections/welmed-inc/5fae2446-4e4b-4238-8a99-a7388bc40eaf) — classification: No Action Indicated (NAI), source: FDA, date: August 30, 2017

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