# Blend Mark LLC - Inspection Records

Source: https://www.globalkeysolutions.net/companies/blend-mark-llc/2bc4d878-2a5c-4c9f-b3ce-3be8a92019f9

> Inspection records and compliance data for Blend Mark LLC in Harvey, Louisiana. Access full analysis and detailed observations.

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## Details

- Name: Blend Mark LLC
- FEI Number: 3006135447
- City: Harvey
- State: Louisiana
- Country Name: United States
- Address Line 1: 2620 8th St
- Zip Code: 70058

## Related Documents

- [FDA Inspection 1286247 - Blend Mark LLC - 2026-03-06](https://www.globalkeysolutions.net/records/fda_inspections/blend-mark-llc/ea23af39-3aa1-4e9b-87d3-3a7851131467) — source: FDA, date: March 6, 2026
- [FDA Inspection 975425 - Blend Mark LLC - 2016-05-24](https://www.globalkeysolutions.net/records/fda_inspections/blend-mark-llc/8d76c01e-e91f-4878-aafd-e91315a4089e) — classification: No Action Indicated (NAI), source: FDA, date: May 24, 2016
- [FDA Inspection 975425 - Blend Mark LLC - 2016-05-24](https://www.globalkeysolutions.net/records/fda_inspections/blend-mark-llc/aee16c29-cd57-46b8-8182-dbc489f77374) — classification: No Action Indicated (NAI), source: FDA, date: May 24, 2016
- [FDA Inspection 975425 - Blend Mark LLC - 2016-05-24](https://www.globalkeysolutions.net/records/fda_inspections/blend-mark-llc/ccd945a2-e1ac-4ff2-892a-74a7b93fa6d4) — classification: No Action Indicated (NAI), source: FDA, date: May 24, 2016
- [FDA Inspection 794836 - Blend Mark LLC - 2012-02-15](https://www.globalkeysolutions.net/records/fda_inspections/blend-mark-llc/c912f69f-9c3a-4b5a-902c-26187d6792f5) — classification: No Action Indicated (NAI), source: FDA, date: February 15, 2012
- [FDA Inspection 794836 - Blend Mark LLC - 2012-02-15](https://www.globalkeysolutions.net/records/fda_inspections/blend-mark-llc/7393a302-cef7-43f6-b363-06d51d441190) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 15, 2012
- [FDA Inspection 794836 - Blend Mark LLC - 2012-02-15](https://www.globalkeysolutions.net/records/fda_inspections/blend-mark-llc/3897e91a-5cda-44a6-8d42-0a265f2504df) — classification: No Action Indicated (NAI), source: FDA, date: February 15, 2012

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