# American Thermal Instruments Inc, Moraine, OH – FDA Inspections

Source: https://www.keypedia.com/companies/american-thermal-instruments-inc/fc83d7d9-be98-4084-8bfb-be7dcc903bd9

> Inspection records and compliance data for American Thermal Instruments Inc in Moraine, Ohio. 4 FDA inspections on record, 1 Form 483, last inspected October 20, 2023.

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## Details

- Name: American Thermal Instruments Inc
- FEI Number: 1526410
- Address Line 1: 2400 E River Rd
- City: Moraine
- State: Ohio
- Zip Code: 45439
- Country Name: United States
- Address: 2400 E River Rd, Moraine, Ohio 45439, United States
- Country: United States

## Related Documents

- FDA Inspection 1220967 - American Thermal Instruments Inc - 2023-10-20 — classification: No Action Indicated (NAI), source: FDA, date: October 20, 2023
- [EIR - American Thermal Instruments Inc - 2022-03-14](https://www.keypedia.com/records/eir/american-thermal-instruments-inc/3e64d33c-8a0a-45f7-9d0b-9799811b24f8) — source: FDA, date: March 14, 2022
- [483 - American Thermal Instruments Inc - 2022-03-14](https://www.keypedia.com/records/483/american-thermal-instruments-inc/219eb3c8-f07f-4d14-861b-68c72f7aac23) — source: FDA, date: March 14, 2022
- [FDA Inspection 1164523 - American Thermal Instruments Inc - 2022-03-14](https://www.keypedia.com/records/fda_inspections/american-thermal-instruments-inc/847c2d54-cc06-46b8-8e7d-07e952bafe21) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 14, 2022
- [FDA Inspection 1043192 - American Thermal Instruments Inc - 2018-03-01](https://www.keypedia.com/records/fda_inspections/american-thermal-instruments-inc/6bba78df-1b1c-401b-a3b5-bab36124e770) — classification: No Action Indicated (NAI), source: FDA, date: March 1, 2018
- FDA Inspection 1043192 - American Thermal Instruments Inc - 2018-03-01 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 1, 2018
- FDA Inspection 715596 - American Thermal Instruments Inc - 2011-03-14 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 14, 2011

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