# FDA Inspection 987569 - LIFESCAN EUROPE GMBH - August 08, 2016

Source: https://www.keypedia.com/records/fda_inspections/lifescan-europe-gmbh/7748507b-2f30-4591-b8ac-228a2fa9bf49
Source feed: FDA_Inspections

> FDA Inspection 987569 for LIFESCAN EUROPE GMBH on August 08, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 987569
- Company Name: LIFESCAN EUROPE GMBH
- Inspection Date: 2016-08-08
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 867956 - 2014-02-12](https://www.keypedia.com/records/fda_inspections/lifescan-europe-gmbh/917d2479-9e1b-4e1a-a1ba-daac3b6e98a9)

Company: https://www.keypedia.com/companies/lifescan-europe-gmbh/5494648d-6568-4272-9605-2441370a5d43

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