# FDA Inspection 1194244 - Lowell, Inc. - December 06, 2022

Source: https://www.globalkeysolutions.net/records/fda_inspections/lowell-inc/df02af65-7d6d-47db-890d-9ad5e08e8091
Source feed: FDA_Inspections

> FDA Inspection 1194244 for Lowell, Inc. on December 06, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1194244
- Company Name: Lowell, Inc.
- Inspection Date: 2022-12-06
- 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 1194244 - 2022-12-06](https://www.globalkeysolutions.net/records/fda_inspections/lowell-inc/2d748cfb-b600-4bd7-be66-f5e68ce1e261)
- [FDA Inspection 1004052 - 2017-03-10](https://www.globalkeysolutions.net/records/fda_inspections/lowell-inc/9ebac319-233e-42d1-83d5-3c95e0cad7a3)
- [FDA Inspection 1004052 - 2017-03-10](https://www.globalkeysolutions.net/records/fda_inspections/lowell-inc/b1eca052-796a-42ea-9268-c08fe46f4778)
- [FDA Inspection 729519 - 2011-06-08](https://www.globalkeysolutions.net/records/fda_inspections/lowell-inc/700a4904-4f77-4ea6-910b-4101c375a999)

Company: https://www.globalkeysolutions.net/companies/lowell-inc/c3435694-b207-45cf-90bf-845a2ab54843

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