# Riensch & Held GmbH & Co KG – FDA Inspection, Aug 24, 2017

Source: https://www.keypedia.com/records/fda_inspections/riensch-held-gmbh-co-kg/9a959c98-58fb-40a0-86cf-ebc6b571c0db
Source feed: FDA_Inspections

> FDA inspection 1022682 of Riensch & Held GmbH & Co KG, August 24, 2017. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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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: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1205445 - 2023-04-19

## Related Officers

- Teresa K. Kastner

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

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