# FDA Inspection 552372 - Rhytec Inc. - December 15, 2008

Source: https://www.keypedia.com/records/fda_inspections/rhytec-inc/2a3fd51a-3114-465c-bbf5-5747c0452217
Source feed: FDA_Inspections

> FDA Inspection 552372 for Rhytec Inc. on December 15, 2008. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 552372
- Company Name: Rhytec Inc.
- Inspection Date: 2008-12-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/rhytec-inc/bfd66624-7aba-409f-98cd-479527f1ec35

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