# FDA Inspection 1249545 - EPflex Feinwerktechnik GmbH - September 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 for EPflex Feinwerktechnik GmbH on September 19, 2024. Classification: No Action Indicated (NAI).

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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)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations

## Related Documents

- [FDA Inspection 1249545 - 2024-09-19](https://www.keypedia.com/records/fda_inspections/epflex-feinwerktechnik-gmbh/838070de-1de7-4cee-81f0-e1baa6b2fee3)
- [FDA Inspection 1249545 - 2024-09-19](https://www.keypedia.com/records/fda_inspections/epflex-feinwerktechnik-gmbh/d4c4be1b-ff6f-49fe-9657-281f747c207f)
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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)
- [FDA Inspection 921735 - 2015-02-26](https://www.keypedia.com/records/fda_inspections/epflex-feinwerktechnik-gmbh/05148442-73ac-47fa-a7c5-27766f55440a)

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