# FDA Inspection 1001740 - Edward M. Geltman, MD - January 30, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/edward-m-geltman-md/f991fb42-916b-4c39-9a62-e89891ee1b1e/
Source feed: FDA_Inspections

> FDA Inspection 1001740 for Edward M. Geltman, MD on January 30, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1001740
- Company Name: Edward M. Geltman, MD
- Inspection Date: 2017-01-30
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 959257 - 2016-02-12](https://www.globalkeysolutions.net/api/records/fda_inspections/edward-m-geltman-md/8c4134d8-8334-474c-b9a8-39f13663df65/)

Company: https://www.globalkeysolutions.net/companies/edward-m-geltman-md/876542c6-2327-4173-a2fa-0197b24d23eb

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