FDA Inspection
AMO Manufacturing USA, LLCAMO Manufacturing USA, LLC – FDA Inspection, Sep 29, 2017
Record Details
This FDA Inspection record concerns AMO Manufacturing USA, LLC, with an inspection on September 29, 2017, issued by the San Francisco District Office, covering medical devices & rad health.
- Company
- AMO Manufacturing USA, LLC
- Inspection Date
- September 29, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 025fe10c-bdfa-4ce7-8a1f-30002b161d1c
Inspection Facts
- Inspection number
- 1042521
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of AMO Manufacturing USA, LLC
7| Date | Classification | Office | Project area |
|---|---|---|---|
| September 18, 2019 | Not classified | San Francisco District Office | |
| April 5, 2017 | Not classified | San Francisco District Office | |
| February 4, 2016 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| July 8, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 28, 2013 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for AMO Manufacturing USA, LLC
- FDA Inspection 1123569 - 2019-09-18
- FDA Inspection 1010577 - 2017-04-05
- FDA Inspection 959790 - 2016-02-04
- FDA Inspection 933874 - 2015-07-08
- FDA Inspection 852970 - 2013-10-28
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