# FDA Inspection 1258115 - KLS Martin SE & Co. KG - April 09, 2025

Source: https://www.keypedia.com/records/fda_inspections/kls-martin-se-co-kg/41b77759-e810-4efc-8ee7-4ca976f07130
Source feed: FDA_Inspections

> FDA Inspection 1258115 for KLS Martin SE & Co. KG on April 09, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1258115
- Company Name: KLS Martin SE & Co. KG
- Inspection Date: 2025-04-09
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1258115 - 2025-04-09](https://www.keypedia.com/records/fda_inspections/kls-martin-se-co-kg/7af9a09a-35e7-48ce-b914-d2cbb1bd4300)
- [FDA Inspection 1258115 - 2025-04-09](https://www.keypedia.com/records/fda_inspections/kls-martin-se-co-kg/53e98f51-0521-4ae1-af4c-2120366d9830)
- [FDA Inspection 750308 - 2011-09-28](https://www.keypedia.com/records/fda_inspections/kls-martin-se-co-kg/d2799d74-6d3c-4cb8-9d60-c84baf561fd0)
- [FDA Inspection 750308 - 2011-09-28](https://www.keypedia.com/records/fda_inspections/kls-martin-se-co-kg/5a2214d9-cda4-44c1-b160-d53610b02520)

Company: https://www.keypedia.com/companies/kls-martin-se-co-kg/3ea282e3-9eda-4389-940a-399a1c20e4c6

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