# AMD Medicom Inc. (GRANBY PLANT) – FDA Inspection, Feb 9, 2017

Source: https://www.keypedia.com/records/fda_inspections/amd-medicom-inc-granby-plant/9ccb46e0-6778-49b1-8fa5-ac6bef4dfa6e
Source feed: FDA_Inspections

> FDA inspection 1001543 of AMD Medicom Inc. (GRANBY PLANT), February 09, 2017. Classification: No Action Indicated (NAI). 3 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1001543
- Company Name: AMD Medicom Inc. (GRANBY PLANT)
- Inspection Date: 2017-02-09
- 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: 3

## Related Documents

- FDA Inspection 820366 - 2013-02-14
- FDA Inspection 584594 - 2009-05-08

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/frank-j-marciniak/6995351a-6afc-4056-9692-d4aeb711dd92)

Company: https://www.keypedia.com/companies/amd-medicom-inc-granby-plant/115c75c3-def5-46a6-b7e4-101731219042

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