# FDA Inspection 1249760 - DELBio (Wujiang) Co., Ltd. - September 12, 2024

Source: https://www.keypedia.com/records/fda_inspections/delbio-wujiang-co-ltd/4e013414-d0ac-4efc-8a80-7c610c60c062
Source feed: FDA_Inspections

> FDA Inspection 1249760 for DELBio (Wujiang) Co., Ltd. on September 12, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1249760
- Company Name: DELBio (Wujiang) Co., Ltd.
- Inspection Date: 2024-09-12
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations

## Related Documents

- [FDA Inspection 1249760 - 2024-09-12](https://www.keypedia.com/records/fda_inspections/delbio-wujiang-co-ltd/0e30e342-d6ce-42d0-876d-5d628c0d3b17)
- [FDA Inspection 1249760 - 2024-09-12](https://www.keypedia.com/records/fda_inspections/delbio-wujiang-co-ltd/09640b0c-0167-4f82-9328-ba6eb3f8ac19)
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Company: https://www.keypedia.com/companies/delbio-wujiang-co-ltd/9b90c95b-a3bb-46b3-ac70-0b839a576835

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8