# FDA Inspection 1068032 - PEROUSE MEDICAL - July 18, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/perouse-medical/eea99654-8e05-4f45-b267-14e9514d9cca
Source feed: FDA_Inspections

> FDA Inspection 1068032 for PEROUSE MEDICAL on July 18, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1068032
- Company Name: PEROUSE MEDICAL
- Inspection Date: 2018-07-18
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/perouse-medical/5b7b6557-e9d0-4fc6-bb38-04de00342294

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