# FDA Inspection 897633 - Brasseler USA I Lp - September 29, 2014

Source: https://www.keypedia.com/records/fda_inspections/brasseler-usa-i-lp/2068b1a4-6fef-4f58-89e4-8616da1b2ea9
Source feed: FDA_Inspections

> FDA Inspection 897633 for Brasseler USA I Lp on September 29, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 897633
- Company Name: Brasseler USA I Lp
- Inspection Date: 2014-09-29
- 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 897633 - 2014-09-29](https://www.keypedia.com/records/fda_inspections/brasseler-usa-i-lp/f2886dbc-b7c8-46d6-908b-ad7ef278dc5c)
- [FDA Inspection 694866 - 2010-10-21](https://www.keypedia.com/records/fda_inspections/brasseler-usa-i-lp/055efb68-b711-49c7-b12d-62da9dd3838a)
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Company: https://www.keypedia.com/companies/brasseler-usa-i-lp/a8dfb2fa-89ec-4a27-a22f-1fae99e3ae28

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