# Fehling Instruments GmbH & Co. KG – FDA Inspection, Jun 18, 2015

Source: https://www.keypedia.com/records/fda_inspections/fehling-instruments-gmbh-co-kg/76741153-7cde-48d1-96ed-2f967bdfddc8
Source feed: FDA_Inspections

> FDA inspection 933817 of Fehling Instruments GmbH & Co. KG, June 18, 2015. Classification: Official Action Indicated (OAI). 9 citations under 21 CFR parts 803, 806 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 933817
- Company Name: Fehling Instruments GmbH & Co. KG
- Inspection Date: 2015-06-18
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 9

## Related Documents

- [FDA Inspection 1306904 - 2026-03-12](https://www.keypedia.com/records/fda_inspections/fehling-instruments-gmbh-co-kg/d608f7d3-a8a4-41d9-99f4-8ed91926214f)
- FDA Inspection 1097118 - 2019-05-23

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