# FDA Inspection 1022940 - Mak-System Corp. - August 03, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/mak-system-corp/8dbaf2db-9c45-4417-a9a5-341cfe3f3679/
Source feed: FDA_Inspections

> FDA Inspection 1022940 for Mak-System Corp. on August 03, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1022940
- Company Name: Mak-System Corp.
- Inspection Date: 2017-08-03
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/mak-system-corp/7fadbd95-9e72-4d4e-aec3-7ef67f463ff6

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7