# FDA Inspection 850711 - Berchtold Corp. - September 23, 2013

Source: https://www.keypedia.com/records/fda_inspections/berchtold-corp/f07ff8bf-977a-48d4-a011-bf5d28f53222
Source feed: FDA_Inspections

> FDA Inspection 850711 for Berchtold Corp. on September 23, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 850711
- Company Name: Berchtold Corp.
- Inspection Date: 2013-09-23
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 850711 - 2013-09-23](https://www.keypedia.com/records/fda_inspections/berchtold-corp/a79b1757-105d-4266-bdf0-34239f1b821a)
- [FDA Inspection 643962 - 2010-02-04](https://www.keypedia.com/records/fda_inspections/berchtold-corp/40e570c0-bf1c-46d6-b6bb-004506cbbf71)
- [FDA Inspection 643962 - 2010-02-04](https://www.keypedia.com/records/fda_inspections/berchtold-corp/5b157b60-efea-4193-b296-aa16e56c8428)

Company: https://www.keypedia.com/companies/berchtold-corp/a96587f5-0946-4dce-93b0-2069ecfba6d8

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