# FDA Inspection 1022682 - Riensch & Held GmbH & Co KG - August 24, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/riensch-held-gmbh-co-kg/0baceb76-da56-432e-a8f3-f2a39d5d523a
Source feed: FDA_Inspections

> FDA Inspection 1022682 for Riensch & Held GmbH & Co KG on August 24, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1022682
- Company Name: Riensch & Held GmbH & Co KG
- Inspection Date: 2017-08-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1022682 - 2017-08-24](https://www.globalkeysolutions.net/records/fda_inspections/riensch-held-gmbh-co-kg/9a959c98-58fb-40a0-86cf-ebc6b571c0db)

Company: https://www.globalkeysolutions.net/companies/riensch-held-gmbh-co-kg/33a91ab4-8d5e-4e42-877d-b0dbf75790ab

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