# EPflex Feinwerktechnik GmbH – FDA Inspection, Sep 19, 2024

Source: https://www.keypedia.com/records/fda_inspections/epflex-feinwerktechnik-gmbh/7bf05d18-44bc-43f8-9364-fe80723bc1bc
Source feed: FDA_Inspections

> FDA inspection 1249545 of EPflex Feinwerktechnik GmbH, September 19, 2024. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1249545
- Company Name: EPflex Feinwerktechnik GmbH
- Inspection Date: 2024-09-19
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 2

## Related Documents

- [FDA Inspection 921735 - 2015-02-26](https://www.keypedia.com/records/fda_inspections/epflex-feinwerktechnik-gmbh/c9fe4e65-afba-4b98-a507-1c7e29ef235f)
- [FDA Inspection 839372 - 2013-06-13](https://www.keypedia.com/records/fda_inspections/epflex-feinwerktechnik-gmbh/a26f4392-a27e-4d8a-9e6e-a8b0b5d37dfb)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/james-r-montero/ce2d19fd-25b7-423e-9132-5d6f582380d2)

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

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8