# FDA Inspection 897771 - Nor-Lake, Inc. - September 04, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/nor-lake-inc/c33e6f4f-07a3-42b7-b242-a9af99061bc5
Source feed: FDA_Inspections

> FDA Inspection 897771 for Nor-Lake, Inc. on September 04, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 897771
- Company Name: Nor-Lake, Inc.
- Inspection Date: 2014-09-04
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1046453 - 2018-03-13](https://www.globalkeysolutions.net/records/fda_inspections/nor-lake-inc/69c0968e-bb75-443e-802b-92d30cd44e97)

Company: https://www.globalkeysolutions.net/companies/nor-lake-inc/e889cefc-abb7-4c76-b8b1-119ca5cdbcca

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