# FDA Inspection 754500 - Reichert, Inc. - November 22, 2011

Source: https://www.keypedia.com/records/fda_inspections/reichert-inc/0c7f0588-234b-4d58-85e2-4bccb418dfde
Source feed: FDA_Inspections

> FDA Inspection 754500 for Reichert, Inc. on November 22, 2011. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 754500
- Company Name: Reichert, Inc.
- Inspection Date: 2011-11-22
- 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/ef1878ec-52b3-446e-b31d-bfec2ae52f9e)
- [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)

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