# FDA Inspection 1097118 - Fehling Instruments GmbH & Co. KG - May 23, 2019

Source: https://www.keypedia.com/records/fda_inspections/fehling-instruments-gmbh-co-kg/398ee7af-512b-4e20-87c1-cbcd03b98e74
Source feed: FDA_Inspections

> FDA Inspection 1097118 for Fehling Instruments GmbH & Co. KG on May 23, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1097118
- Company Name: Fehling Instruments GmbH & Co. KG
- Inspection Date: 2019-05-23
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/fehling-instruments-gmbh-co-kg/5de69c57-56e8-4569-8e3e-8816ce90532e

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