# FDA Inspection 1023288 - BTI Filtration - August 24, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/bti-filtration/bdf92c3d-882b-491d-8af6-a8f51733b171
Source feed: FDA_Inspections

> FDA Inspection 1023288 for BTI Filtration on August 24, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1023288
- Company Name: BTI Filtration
- Inspection Date: 2017-08-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/bti-filtration/adf592c1-58a3-4de5-859e-a70fe9dba818

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