# FDA Inspection 1211404 - InVitroCare, Inc - August 03, 2023

Source: https://www.keypedia.com/records/fda_inspections/invitrocare-inc/c50556d4-0809-40f2-88ec-80387bb91d30
Source feed: FDA_Inspections

> FDA Inspection 1211404 for InVitroCare, Inc on August 03, 2023. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1211404
- Company Name: InVitroCare, Inc
- Inspection Date: 2023-08-03
- 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 1211404 - 2023-08-03](https://www.keypedia.com/records/fda_inspections/invitrocare-inc/2ab2068e-d3e9-4837-b749-5a57abb768ae)
- [FDA Inspection 800358 - 2012-09-25](https://www.keypedia.com/records/fda_inspections/invitrocare-inc/90632397-6421-4038-9a53-099d30993480)
- [FDA Inspection 800358 - 2012-09-25](https://www.keypedia.com/records/fda_inspections/invitrocare-inc/b477ff4d-c09e-4374-b3c3-a4079fd164ff)

Company: https://www.keypedia.com/companies/invitrocare-inc/55a32e03-0d2e-42fc-9c82-ff2ce97b2d33

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