# Medline Industries LP - Inspection Records

Source: https://www.globalkeysolutions.net/companies/medline-industries-lp/a2a0aba0-4dd1-45ab-be38-15ce7d1824dc

> Inspection records and compliance data for Medline Industries LP in Laredo, Texas. Access full analysis and detailed observations.

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## Details

- Name: Medline Industries LP
- FEI Number: 3005595283
- City: Laredo
- State: Texas
- Country Name: United States
- Address Line 1: 12001 General Milton
- Zip Code: 78045

## Related Documents

- [FDA Inspection 1231389 - Medline Industries LP - 2024-01-29](https://www.globalkeysolutions.net/records/fda_inspections/medline-industries-lp/e80643fe-bcf6-4ca6-9b59-0274183541b4) — classification: No Action Indicated (NAI), source: FDA, date: January 29, 2024
- [FDA Inspection 1043290 - Medline Industries LP - 2017-11-01](https://www.globalkeysolutions.net/records/fda_inspections/medline-industries-lp/d470248d-05ab-4ddb-bf13-cd4fcba397d9) — classification: No Action Indicated (NAI), source: FDA, date: November 1, 2017
- [FDA Inspection 1043290 - Medline Industries LP - 2017-11-01](https://www.globalkeysolutions.net/records/fda_inspections/medline-industries-lp/d20af418-3765-4f3e-b835-87a8cf8ed0a0) — classification: No Action Indicated (NAI), source: FDA, date: November 1, 2017
- [FDA Inspection 928486 - Medline Industries LP - 2015-06-01](https://www.globalkeysolutions.net/records/fda_inspections/medline-industries-lp/bcaa7ed6-bcb7-4177-9b48-4e02935a2af6) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 1, 2015
- [FDA Inspection 928486 - Medline Industries LP - 2015-06-01](https://www.globalkeysolutions.net/records/fda_inspections/medline-industries-lp/71e46614-9f29-4f99-a414-1dee44ca465e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 1, 2015
- [FDA Inspection 595311 - Medline Industries LP - 2009-06-17](https://www.globalkeysolutions.net/records/fda_inspections/medline-industries-lp/df61b49f-193b-451b-bcf9-c0154585ffae) — classification: No Action Indicated (NAI), source: FDA, date: June 17, 2009

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