# Bernstein AG – FDA Inspection, Feb 26, 2009

Source: https://www.keypedia.com/records/fda_inspections/bernstein-ag/7099bf31-34d4-4939-ac9c-69e8a3e20fe6
Source feed: FDA_Inspections

> FDA inspection 569728 of Bernstein AG, February 26, 2009. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 569728
- Company Name: Bernstein AG
- Inspection Date: 2009-02-26
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 994375 - 2016-11-10

Company: https://www.keypedia.com/companies/bernstein-ag/11527cf1-c60d-47ad-92aa-1a303c8d1e23

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