# FDA Inspection 1203814 - Teledyne Analytical Instruments - April 25, 2023

Source: https://www.keypedia.com/records/fda_inspections/teledyne-analytical-instruments/4ffd917a-bd8b-4efa-90b7-d65dd3de80e8
Source feed: FDA_Inspections

> FDA Inspection 1203814 for Teledyne Analytical Instruments on April 25, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1203814
- Company Name: Teledyne Analytical Instruments
- Inspection Date: 2023-04-25
- 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 1203814 - 2023-04-25](https://www.keypedia.com/records/fda_inspections/teledyne-analytical-instruments/2bd51ac8-35c6-4a16-899a-8b2c4eaeedb6)
- [FDA Inspection 1016446 - 2017-06-30](https://www.keypedia.com/records/fda_inspections/teledyne-analytical-instruments/1502fe29-f55a-4611-a174-c2641c5d6f5d)
- [FDA Inspection 1016446 - 2017-06-30](https://www.keypedia.com/records/fda_inspections/teledyne-analytical-instruments/c3a96c64-a851-43b8-ac1d-8eeafa2096d4)

Company: https://www.keypedia.com/companies/teledyne-analytical-instruments/441a819c-60fc-4690-b53f-ac4ff51e806d

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