# FDA Inspection 1228305 - Gold Coast IVF - January 31, 2024

Source: https://www.globalkeysolutions.net/records/fda_inspections/gold-coast-ivf/fb1162cd-6997-41ae-97d4-d1e935f64208/
Source feed: FDA_Inspections

> FDA Inspection 1228305 for Gold Coast IVF on January 31, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1228305
- Company Name: Gold Coast IVF
- Inspection Date: 2024-01-31
- Classification: No Action Indicated (NAI)
- Project Area: Blood and Blood Products
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

## Related Documents

- [FDA Inspection 1228305 - 2024-01-31](https://www.globalkeysolutions.net/api/records/fda_inspections/gold-coast-ivf/3279999f-5fe3-4fc1-a38d-dc2a98341abb/)
- [FDA Inspection 1162321 - 2022-02-14](https://www.globalkeysolutions.net/api/records/fda_inspections/gold-coast-ivf/098d9329-fee1-42dc-864e-514d436b4825/)
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- [FDA Inspection 1070962 - 2018-10-17](https://www.globalkeysolutions.net/api/records/fda_inspections/gold-coast-ivf/5082a414-c41d-409e-9abc-3d313b268cae/)

Company: https://www.globalkeysolutions.net/companies/gold-coast-ivf/82d4ccdd-e388-4215-808d-9a9060340d7a

Office: https://www.globalkeysolutions.net/offices/center-for-biologics-evaluation-and-research/dd9e8ea7-6f04-4ed1-b0d7-e7e6b264570d
