# I.E.M. Gmbh – FDA Inspection, Oct 21, 2011

Source: https://www.keypedia.com/records/fda_inspections/iem-gmbh/83009436-6669-4709-bce1-48bbd14e00a7
Source feed: FDA_Inspections

> FDA inspection 753156 of I.E.M. Gmbh, October 21, 2011. Classification: Official Action Indicated (OAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 753156
- Company Name: I.E.M. Gmbh
- Inspection Date: 2011-10-21
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 818868 - 2013-01-24
- FDA Inspection 571413 - 2009-02-19

Company: https://www.keypedia.com/companies/iem-gmbh/bcf2e861-d4d8-4616-8af7-f5c543ef964d

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