# FDA Inspection 997641 - Heidelberg Engineering - January 20, 2017

Source: https://www.keypedia.com/records/fda_inspections/heidelberg-engineering/a8989ef4-b8de-4495-98df-a1f33ad46299
Source feed: FDA_Inspections

> FDA Inspection 997641 for Heidelberg Engineering on January 20, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 997641
- Company Name: Heidelberg Engineering
- Inspection Date: 2017-01-20
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/heidelberg-engineering/7801b73e-ca03-4441-b4b5-72db99c0b7e1

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