# Reichert, Inc. – FDA Inspection, Apr 28, 2017

Source: https://www.keypedia.com/records/fda_inspections/reichert-inc/ef1878ec-52b3-446e-b31d-bfec2ae52f9e
Source feed: FDA_Inspections

> FDA inspection 1010616 of Reichert, Inc., April 28, 2017. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1010616
- Company Name: Reichert, Inc.
- Inspection Date: 2017-04-28
- 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: 4

## Related Documents

- FDA Inspection 754500 - 2011-11-22

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/matthew-d-schnittker/cf76f07f-db6d-47a0-8412-7eb084d4fe8b)

Company: https://www.keypedia.com/companies/reichert-inc/2fb7ca2c-08c4-4ba0-9bc8-da0d7e9919dd

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