# FDA Inspection 1010616 - Reichert, Inc. - April 28, 2017

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

> FDA Inspection 1010616 for Reichert, Inc. on April 28, 2017. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1010616 - 2017-04-28](https://www.keypedia.com/records/fda_inspections/reichert-inc/6f9035d5-0485-47e2-bf87-b9eb88aacc12)
- [FDA Inspection 754500 - 2011-11-22](https://www.keypedia.com/records/fda_inspections/reichert-inc/3302b1fe-6852-49a5-a945-7588feb961cf)
- [FDA Inspection 754500 - 2011-11-22](https://www.keypedia.com/records/fda_inspections/reichert-inc/0c7f0588-234b-4d58-85e2-4bccb418dfde)

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