# AMO Manufacturing USA, LLC – FDA Inspection, Oct 28, 2013

Source: https://www.keypedia.com/records/fda_inspections/amo-manufacturing-usa-llc/95d58d3d-67fc-4372-b466-cc3cb567754e
Source feed: FDA_Inspections

> FDA inspection 852970 of AMO Manufacturing USA, LLC, October 28, 2013. Classification: No Action Indicated (NAI). 7 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 852970
- Company Name: AMO Manufacturing USA, LLC
- Inspection Date: 2013-10-28
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1123569 - 2019-09-18
- [FDA Inspection 1042521 - 2017-09-29](https://www.keypedia.com/records/fda_inspections/amo-manufacturing-usa-llc/025fe10c-bdfa-4ce7-8a1f-30002b161d1c)
- FDA Inspection 1010577 - 2017-04-05
- [FDA Inspection 959790 - 2016-02-04](https://www.keypedia.com/records/fda_inspections/amo-manufacturing-usa-llc/a1760042-3f62-466a-9a77-48e51b59e13c)
- FDA Inspection 933874 - 2015-07-08

Company: https://www.keypedia.com/companies/amo-manufacturing-usa-llc/64836d88-5789-46b2-8ddd-8a3bb8602ef3

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