# FDA Inspection 1114837 - Heinz Reiske - December 05, 2019

Source: https://www.keypedia.com/records/fda_inspections/heinz-reiske/200f0dc9-09b7-4e60-b18b-9f4058acfc4b
Source feed: FDA_Inspections

> FDA Inspection 1114837 for Heinz Reiske on December 05, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1114837
- Company Name: Heinz Reiske
- Inspection Date: 2019-12-05
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/heinz-reiske/235283a8-65a8-4c90-b1ac-7855aebf3500

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