# EPflex Feinwerktechnik GmbH – FDA Inspection, Jun 13, 2013

Source: https://www.keypedia.com/records/fda_inspections/epflex-feinwerktechnik-gmbh/a26f4392-a27e-4d8a-9e6e-a8b0b5d37dfb
Source feed: FDA_Inspections

> FDA inspection 839372 of EPflex Feinwerktechnik GmbH, June 13, 2013. Classification: Official Action Indicated (OAI). 7 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 839372
- Company Name: EPflex Feinwerktechnik GmbH
- Inspection Date: 2013-06-13
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 7

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- [FDA Inspection 921735 - 2015-02-26](https://www.keypedia.com/records/fda_inspections/epflex-feinwerktechnik-gmbh/c9fe4e65-afba-4b98-a507-1c7e29ef235f)

Company: https://www.keypedia.com/companies/epflex-feinwerktechnik-gmbh/7523fecf-a471-4e7e-925a-d0f40c42be9f

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