# FDA Inspection 1069138 - SARSTEDT AG & CO. KG - September 20, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/sarstedt-ag-co-kg/6b64c24e-8acd-4ae3-9189-84858a451698
Source feed: FDA_Inspections

> FDA Inspection 1069138 for SARSTEDT AG & CO. KG on September 20, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1069138
- Company Name: SARSTEDT AG & CO. KG
- Inspection Date: 2018-09-20
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1069138 - 2018-09-20](https://www.globalkeysolutions.net/records/fda_inspections/sarstedt-ag-co-kg/4f331bb0-24e8-4c16-a757-be29fec1fe61)
- [FDA Inspection 998278 - 2016-11-04](https://www.globalkeysolutions.net/records/fda_inspections/sarstedt-ag-co-kg/2f80b13c-64b7-4852-8a2b-782c71f82a14)

Company: https://www.globalkeysolutions.net/companies/sarstedt-ag-co-kg/f24de9f4-24d1-4bf7-90f8-c928b9c55076

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