# KLS Martin SE & Co. KG – FDA Inspection, Sep 28, 2011

Source: https://www.keypedia.com/records/fda_inspections/kls-martin-se-co-kg/d2799d74-6d3c-4cb8-9d60-c84baf561fd0
Source feed: FDA_Inspections

> FDA inspection 750308 of KLS Martin SE & Co. KG, September 28, 2011. Classification: Voluntary Action Indicated (VAI). 3 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: 750308
- Company Name: KLS Martin SE & Co. KG
- Inspection Date: 2011-09-28
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 1258115 - 2025-04-09
- FDA Inspection 1067685 - 2018-08-23

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