# FDA Inspection 891089 - MAXTER CATHETERS - July 31, 2014

Source: https://www.keypedia.com/records/fda_inspections/maxter-catheters/957be67b-0a21-4e24-afad-88f61a6730e8
Source feed: FDA_Inspections

> FDA Inspection 891089 for MAXTER CATHETERS on July 31, 2014. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 891089
- Company Name: MAXTER CATHETERS
- Inspection Date: 2014-07-31
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/maxter-catheters/7545fab6-9e8d-4913-b47b-f95f7f9561e3

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