# FDA Inspection 925313 - Sarstedt Inc - April 16, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/sarstedt-inc/1feb4b8a-bb32-4000-b10f-aa969aff977b
Source feed: FDA_Inspections

> FDA Inspection 925313 for Sarstedt Inc on April 16, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 925313
- Company Name: Sarstedt Inc
- Inspection Date: 2015-04-16
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1057766 - 2018-07-02](https://www.globalkeysolutions.net/records/fda_inspections/sarstedt-inc/2f0e85bb-6ee2-4003-8086-2f94331423f1)
- [FDA Inspection 1057766 - 2018-07-02](https://www.globalkeysolutions.net/records/fda_inspections/sarstedt-inc/5483b23b-2253-43e7-9271-a984de49e042)

Company: https://www.globalkeysolutions.net/companies/sarstedt-inc/f4ac9de6-987b-495b-a99e-5dddb8263e3f

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