# FDA Inspection 917299 - ERKA, KALLMEYER MEDIZINTECHNIK GMBH & CO. KG - March 10, 2015

Source: https://www.keypedia.com/records/fda_inspections/erka-kallmeyer-medizintechnik-gmbh-co-kg/84ea0057-7b77-40e3-8974-2ec6fd905dec
Source feed: FDA_Inspections

> FDA Inspection 917299 for ERKA, KALLMEYER MEDIZINTECHNIK GMBH & CO. KG on March 10, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 917299
- Company Name: ERKA, KALLMEYER MEDIZINTECHNIK GMBH & CO. KG
- Inspection Date: 2015-03-10
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/erka-kallmeyer-medizintechnik-gmbh-co-kg/4c54cbeb-58f3-4618-888f-54df0d34db09

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