# FDA Inspection 1202095 - BERGER & KRAFT - March 30, 2023

Source: https://www.keypedia.com/records/fda_inspections/berger-kraft/1bf17879-d7b3-4007-ab40-a1b274f22bfd
Source feed: FDA_Inspections

> FDA inspection 1202095 of BERGER & KRAFT, March 30, 2023. Classification: Voluntary Action Indicated (VAI). 10 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1202095
- Company Name: BERGER & KRAFT
- Inspection Date: 2023-03-30
- 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: 10

## Related Officers

- [Sargum C. Morgan](https://www.keypedia.com/people/sargum-c-morgan/a769e36a-3382-414a-b9b1-1ebc755c8392)

Company: https://www.keypedia.com/companies/berger-kraft/08e641ce-9e1a-47fa-9a97-4e57b8e053a2

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