# FDA Inspection 848902 - Amperor Inc. - September 18, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/amperor-inc/d4174f21-fa6b-4f62-8dc5-bf6f80dbb8ce
Source feed: FDA_Inspections

> FDA Inspection 848902 for Amperor Inc. on September 18, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 848902
- Company Name: Amperor Inc.
- Inspection Date: 2013-09-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1107895 - 2019-10-29](https://www.globalkeysolutions.net/records/fda_inspections/amperor-inc/ed62dfdd-c311-4945-ac73-f5b7e9f3c12a)
- [FDA Inspection 1107895 - 2019-10-29](https://www.globalkeysolutions.net/records/fda_inspections/amperor-inc/ddb6778c-627e-4c4e-abab-e97c710bca4c)
- [FDA Inspection 848902 - 2013-09-18](https://www.globalkeysolutions.net/records/fda_inspections/amperor-inc/4a9a8579-58d8-4dc9-9e4b-b719bafd8ba9)

Company: https://www.globalkeysolutions.net/companies/amperor-inc/a9b7f013-013a-4b96-9175-47da7587c156

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