# Creative Contract Packaging Corporation, LLC, Aurora, IL – FDA Inspections

Source: https://www.keypedia.com/companies/creative-contract-packaging-corporation-llc/7934770c-eb3c-4c32-95d5-3fbb77b78dce

> Inspection records and compliance data for Creative Contract Packaging Corporation, LLC in Aurora, Illinois. 6 FDA inspections on record, last inspected September 19, 2024.

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## Details

- Name: Creative Contract Packaging Corporation, LLC
- FEI Number: 1000115128
- Address Line 1: 3777 And 3837 Exchange Ave
- City: Aurora
- State: Illinois
- Zip Code: 60504
- Country Name: United States
- Address: 3777 And 3837 Exchange Ave, Aurora, Illinois 60504, United States
- Country: United States

## Related Documents

- [FDA Inspection 1237986 - Creative Contract Packaging Corporation, LLC - 2024-09-19](https://www.keypedia.com/records/fda_inspections/creative-contract-packaging-corporation-llc/ca5293aa-2a55-4896-94fb-6c8ab3e6a5d0) — source: FDA, date: September 19, 2024
- FDA Inspection 1237986 - Creative Contract Packaging Corporation, LLC - 2024-09-19 — classification: No Action Indicated (NAI), source: FDA, date: September 19, 2024
- FDA Inspection 1089791 - Creative Contract Packaging Corporation, LLC - 2019-04-24 — classification: No Action Indicated (NAI), source: FDA, date: April 24, 2019
- FDA Inspection 1089791 - Creative Contract Packaging Corporation, LLC - 2019-04-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 24, 2019
- FDA Inspection 1019210 - Creative Contract Packaging Corporation, LLC - 2017-06-01 — classification: No Action Indicated (NAI), source: FDA, date: June 1, 2017
- FDA Inspection 864416 - Creative Contract Packaging Corporation, LLC - 2014-01-30 — classification: No Action Indicated (NAI), source: FDA, date: January 30, 2014
- FDA Inspection 747168 - Creative Contract Packaging Corporation, LLC - 2011-09-16 — classification: No Action Indicated (NAI), source: FDA, date: September 16, 2011
- FDA Inspection 650346 - Creative Contract Packaging Corporation, LLC - 2010-03-03 — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2010

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