# Mak-System Corp. - Inspection Records

Source: https://www.keypedia.com/companies/mak-system-corp/7fadbd95-9e72-4d4e-aec3-7ef67f463ff6

> Inspection records and compliance data for Mak-System Corp. in Des Plaines, Illinois. Access full analysis and detailed observations.

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## Details

- Name: Mak-System Corp.
- FEI Number: 3000215342
- City: Des Plaines
- State: Illinois
- Country Name: United States
- Address Line 1: 2720 S River Rd Ste 225
- Zip Code: 60018

## Related Documents

- [483 - Mak-System Corp. - 2023-08-11](https://www.keypedia.com/records/483/mak-system-corp/48dbd28d-32e7-48c4-ace0-d92bf83a9029) — source: FDA, date: August 11, 2023
- [FDA Inspection 1214579 - Mak-System Corp. - 2023-08-11](https://www.keypedia.com/records/fda_inspections/mak-system-corp/7e9f8b29-61b2-4aaa-b017-17a97b15b109) — classification: No Action Indicated (NAI), source: FDA, date: August 11, 2023
- [FDA Inspection 1214579 - Mak-System Corp. - 2023-08-11](https://www.keypedia.com/records/fda_inspections/mak-system-corp/508e3d24-2107-42d1-baf4-af9381bed16c) — classification: No Action Indicated (NAI), source: FDA, date: August 11, 2023
- [FDA Inspection 1214579 - Mak-System Corp. - 2023-08-11](https://www.keypedia.com/records/fda_inspections/mak-system-corp/3cce6fb1-c2e7-4df9-aaa8-29509404dc51) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 11, 2023
- [FDA Inspection 1022940 - Mak-System Corp. - 2017-08-03](https://www.keypedia.com/records/fda_inspections/mak-system-corp/af00a417-59b2-45c8-99c6-66aa5d55f143) — classification: No Action Indicated (NAI), source: FDA, date: August 3, 2017
- [FDA Inspection 1022940 - Mak-System Corp. - 2017-08-03](https://www.keypedia.com/records/fda_inspections/mak-system-corp/8dbaf2db-9c45-4417-a9a5-341cfe3f3679) — classification: No Action Indicated (NAI), source: FDA, date: August 3, 2017
- [FDA Inspection 1022940 - Mak-System Corp. - 2017-08-03](https://www.keypedia.com/records/fda_inspections/mak-system-corp/b1bea50e-9fda-44e2-a120-68264581f921) — classification: No Action Indicated (NAI), source: FDA, date: August 3, 2017

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