# FDA Inspection 848010 - Hi Tech Swiss Machining Inc - September 10, 2013

Source: https://www.keypedia.com/records/fda_inspections/hi-tech-swiss-machining-inc/b5ae83f6-8718-4e33-871d-9a0d34357cff
Source feed: FDA_Inspections

> FDA Inspection 848010 for Hi Tech Swiss Machining Inc on September 10, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 848010
- Company Name: Hi Tech Swiss Machining Inc
- Inspection Date: 2013-09-10
- 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 848010 - 2013-09-10](https://www.keypedia.com/records/fda_inspections/hi-tech-swiss-machining-inc/7f45966d-8e26-42d8-81ca-1a1c24c41a61)
- [FDA Inspection 739347 - 2011-08-10](https://www.keypedia.com/records/fda_inspections/hi-tech-swiss-machining-inc/fb1c5b86-776d-474d-8895-561d8b0f19ab)
- [FDA Inspection 739347 - 2011-08-10](https://www.keypedia.com/records/fda_inspections/hi-tech-swiss-machining-inc/add9856b-78ae-437b-a599-4ba2bde01a5b)

Company: https://www.keypedia.com/companies/hi-tech-swiss-machining-inc/b6e41e4d-a2c4-494c-b881-06850dc4302e

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