# FDA Inspection 972353 - Tecan  Schweiz  Ag - April 14, 2016

Source: https://www.keypedia.com/records/fda_inspections/tecan-schweiz-ag/b4360a88-e347-40a6-9b97-21b2eb7bb5a6
Source feed: FDA_Inspections

> FDA Inspection 972353 for Tecan  Schweiz  Ag on April 14, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 972353
- Company Name: Tecan  Schweiz  Ag
- Inspection Date: 2016-04-14
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 972353 - 2016-04-14](https://www.keypedia.com/records/fda_inspections/tecan-schweiz-ag/48434346-4cfa-431e-9cd7-bdd3554fedda)
- [FDA Inspection 972353 - 2016-04-14](https://www.keypedia.com/records/fda_inspections/tecan-schweiz-ag/24ad672d-6434-4276-8cd7-9cec3a56a893)

Company: https://www.keypedia.com/companies/tecan-schweiz-ag/f7a03873-6caa-4a5a-98fb-2beda6269010

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