# FDA Inspection 1226655 - Nalge Nunc International Corporation - January 05, 2024

Source: https://www.keypedia.com/records/fda_inspections/nalge-nunc-international-corporation/24faf7d2-afa2-4a50-9c2d-1afd9b52c26d
Source feed: FDA_Inspections

> FDA Inspection 1226655 for Nalge Nunc International Corporation on January 05, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1226655
- Company Name: Nalge Nunc International Corporation
- Inspection Date: 2024-01-05
- 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 1226655 - 2024-01-05](https://www.keypedia.com/records/fda_inspections/nalge-nunc-international-corporation/2aa9f919-1481-43b0-90bb-983a7c263def)
- [FDA Inspection 1159046 - 2021-12-15](https://www.keypedia.com/records/fda_inspections/nalge-nunc-international-corporation/d63f7aa0-f23c-4c14-99ae-7d28a9860e9d)
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- [FDA Inspection 1067034 - 2018-09-26](https://www.keypedia.com/records/fda_inspections/nalge-nunc-international-corporation/1978982d-6347-4be3-9c60-c70fe274a7f4)

Company: https://www.keypedia.com/companies/nalge-nunc-international-corporation/97763e4a-ce32-4573-a31a-39c58cf76fe3

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