# FDA Inspection 660475 - Ametek, Inc. - April 30, 2010

Source: https://www.keypedia.com/records/fda_inspections/ametek-inc/556e7871-7da4-4ddd-a5c0-8a85a903697b
Source feed: FDA_Inspections

> FDA Inspection 660475 for Ametek, Inc. on April 30, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 660475
- Company Name: Ametek, Inc.
- Inspection Date: 2010-04-30
- 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 660475 - 2010-04-30](https://www.keypedia.com/records/fda_inspections/ametek-inc/a17f8443-14ec-40fb-a446-fa36214674d7)

Company: https://www.keypedia.com/companies/ametek-inc/b99ddecf-54e8-4fed-909c-9975ed8b5c10

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