# Diamond Custom Blending, Inc. dba Mix & Pack - Inspection Records

Source: https://www.keypedia.com/companies/diamond-custom-blending-inc-dba-mix-pack/2d11ad27-3008-4fae-86be-bbc5d14d734f

> Inspection records and compliance data for Diamond Custom Blending, Inc. dba Mix & Pack in Little Rock, Arkansas. Access full analysis and detailed observations.

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## Details

- Name: Diamond Custom Blending, Inc. dba Mix & Pack
- FEI Number: 1000220549
- City: Little Rock
- State: Arkansas
- Country Name: United States
- Address Line 1: 8501 Distribution Dr
- Zip Code: 72209

## Related Documents

- [FDA Inspection 1111183 - Diamond Custom Blending, Inc. dba Mix & Pack - 2019-10-17](https://www.keypedia.com/records/fda_inspections/diamond-custom-blending-inc-dba-mix-pack/d06d0875-28be-4a6b-a152-ef09f2acca93) — classification: No Action Indicated (NAI), source: FDA, date: October 17, 2019
- [FDA Inspection 993208 - Diamond Custom Blending, Inc. dba Mix & Pack - 2016-11-30](https://www.keypedia.com/records/fda_inspections/diamond-custom-blending-inc-dba-mix-pack/4dc200f4-baa1-4304-9421-dc474b9f9533) — classification: No Action Indicated (NAI), source: FDA, date: November 30, 2016
- [FDA Inspection 869132 - Diamond Custom Blending, Inc. dba Mix & Pack - 2014-02-12](https://www.keypedia.com/records/fda_inspections/diamond-custom-blending-inc-dba-mix-pack/aaef1298-931a-4117-b630-1bef06d35436) — classification: No Action Indicated (NAI), source: FDA, date: February 12, 2014
- [FDA Inspection 847073 - Diamond Custom Blending, Inc. dba Mix & Pack - 2013-08-20](https://www.keypedia.com/records/fda_inspections/diamond-custom-blending-inc-dba-mix-pack/a291ad2a-7599-48fb-a3d8-6fe428fac28b) — classification: No Action Indicated (NAI), source: FDA, date: August 20, 2013
- [FDA Inspection 620445 - Diamond Custom Blending, Inc. dba Mix & Pack - 2009-10-06](https://www.keypedia.com/records/fda_inspections/diamond-custom-blending-inc-dba-mix-pack/103b9839-3fe6-4747-b2a8-dbd66a1cdad1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 6, 2009

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