# FDA Inspection 1063730 - Boehringer Ingelheim Fremont, Inc. - August 24, 2018

Source: https://www.keypedia.com/records/fda_inspections/boehringer-ingelheim-fremont-inc/7befebbd-e83d-4ca3-9cff-3f3a24ccd094
Source feed: FDA_Inspections

> FDA Inspection 1063730 for Boehringer Ingelheim Fremont, Inc. on August 24, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1063730
- Company Name: Boehringer Ingelheim Fremont, Inc.
- Inspection Date: 2018-08-24
- 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.keypedia.com/companies/boehringer-ingelheim-fremont-inc/3d7d0ca7-27cd-4223-8ade-7193417c9861

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