# FDA Inspection 622929 - Invivo Corporation - October 14, 2009

Source: https://www.keypedia.com/records/fda_inspections/invivo-corporation/022226a6-25eb-48b5-b6c0-8682c5f4e260
Source feed: FDA_Inspections

> FDA Inspection 622929 for Invivo Corporation on October 14, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 622929
- Company Name: Invivo Corporation
- Inspection Date: 2009-10-14
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 622929 - 2009-10-14](https://www.keypedia.com/records/fda_inspections/invivo-corporation/2a5a032d-7751-40b1-8dca-3adad414fe2c)

Company: https://www.keypedia.com/companies/invivo-corporation/5b3b3927-df79-426b-9ce0-be2701f9c5d5

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