# FDA Inspection 1249799 - Lydia Hernandez, M.D. - September 17, 2024

Source: https://www.globalkeysolutions.net/records/fda_inspections/lydia-hernandez-md/c26dd345-8fbd-42b1-b8f8-8f8c7ae800f6
Source feed: FDA_Inspections

> FDA Inspection 1249799 for Lydia Hernandez, M.D. on September 17, 2024. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1249799
- Company Name: Lydia Hernandez, M.D.
- Inspection Date: 2024-09-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Product Evaluation: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Cincinnati District Office

## Related Documents

- [FDA Inspection 1249799 - 2024-09-17](https://www.globalkeysolutions.net/records/fda_inspections/lydia-hernandez-md/82945024-0b64-4681-b24a-e1b53af6f65e)

Company: https://www.globalkeysolutions.net/companies/lydia-hernandez-md/1a621178-4cff-416f-96c4-904d2edadf46

Office: https://www.globalkeysolutions.net/offices/cincinnati-district-office/b67a0c35-82e3-4176-9039-988378f65c22