# MDM Distributing, LLC - Inspection Records

Source: https://www.globalkeysolutions.net/companies/mdm-distributing-llc/6a497521-d7ab-4f00-904f-63cdb88522eb

> Inspection records and compliance data for MDM Distributing, LLC in Laredo, Texas. Access full analysis and detailed observations.

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## Details

- Name: MDM Distributing, LLC
- FEI Number: 3008047973
- City: Laredo
- State: Texas
- Country Name: United States
- Address Line 1: 307 Market St
- Zip Code: 78040

## Related Documents

- [FDA Inspection 1149227 - MDM Distributing, LLC - 2021-08-04](https://www.globalkeysolutions.net/records/fda_inspections/mdm-distributing-llc/a0f2bef8-9c01-47d1-a0bc-32aa6fa80a00) — classification: No Action Indicated (NAI), source: FDA, date: August 4, 2021
- [FDA Inspection 1023091 - MDM Distributing, LLC - 2017-08-28](https://www.globalkeysolutions.net/records/fda_inspections/mdm-distributing-llc/45bc1093-2b23-44d9-b75f-82403b2ae71f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 28, 2017
- [FDA Inspection 868465 - MDM Distributing, LLC - 2014-01-14](https://www.globalkeysolutions.net/records/fda_inspections/mdm-distributing-llc/8ddb3c3d-67ce-4f96-8fa0-bf571f6369b9) — classification: No Action Indicated (NAI), source: FDA, date: January 14, 2014
- [FDA Inspection 700688 - MDM Distributing, LLC - 2010-12-09](https://www.globalkeysolutions.net/records/fda_inspections/mdm-distributing-llc/ce11a233-0593-410b-8c1e-1d700a9a9238) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 9, 2010
- [FDA Inspection 700688 - MDM Distributing, LLC - 2010-12-09](https://www.globalkeysolutions.net/records/fda_inspections/mdm-distributing-llc/8af85fe4-113e-4565-acd4-27ad84e31582) — classification: No Action Indicated (NAI), source: FDA, date: December 9, 2010
- [FDA Inspection 700688 - MDM Distributing, LLC - 2010-12-09](https://www.globalkeysolutions.net/records/fda_inspections/mdm-distributing-llc/d9948054-bbbd-460d-9e54-31a74dc91fbf) — classification: No Action Indicated (NAI), source: FDA, date: December 9, 2010

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