# Teledyne Analytical Instruments – FDA Inspection, Jun 30, 2017

Source: https://www.keypedia.com/records/fda_inspections/teledyne-analytical-instruments/c3a96c64-a851-43b8-ac1d-8eeafa2096d4
Source feed: FDA_Inspections

> FDA inspection 1016446 of Teledyne Analytical Instruments, June 30, 2017. Classification: Voluntary Action Indicated (VAI). 8 citations under 21 CFR parts 806 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1016446
- Company Name: Teledyne Analytical Instruments
- Inspection Date: 2017-06-30
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 8

## Related Documents

- [FDA Inspection 1203814 - 2023-04-25](https://www.keypedia.com/records/fda_inspections/teledyne-analytical-instruments/4ffd917a-bd8b-4efa-90b7-d65dd3de80e8)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/janet-pulver/d46b01cd-8c3d-4a54-bb91-843e0f94de89)

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