# FDA Inspection 1078512 - Haven Manufacturing - February 07, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/haven-manufacturing/59b61b0d-ff38-4973-8220-6b39ffef7942
Source feed: FDA_Inspections

> FDA Inspection 1078512 for Haven Manufacturing on February 07, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1078512
- Company Name: Haven Manufacturing
- Inspection Date: 2019-02-07
- Classification: Voluntary Action Indicated (VAI)
- 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/haven-manufacturing/e7d195e4-ee72-4d98-bf2e-36b8aeafcd00

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