# ABL Manufacturing, LLC – FDA Inspection, Aug 1, 2017

Source: https://www.keypedia.com/records/fda_inspections/abl-manufacturing-llc/297609d9-9d88-48c5-ae2e-beebc0e4c666
Source feed: FDA_Inspections

> FDA inspection 1024120 of ABL Manufacturing, LLC, August 01, 2017. Classification: No Action Indicated (NAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1024120
- Company Name: ABL Manufacturing, LLC
- Inspection Date: 2017-08-01
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1037971 - 2017-12-08
- FDA Inspection 916439 - 2015-03-03
- FDA Inspection 796037 - 2012-08-23
- [FDA Inspection 717774 - 2011-03-25](https://www.keypedia.com/records/fda_inspections/abl-manufacturing-llc/7f2a5590-7d40-4582-a644-92a018314709)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/daniel-j-lahar/d4e329c0-b6a5-42ca-acde-b79413b245ea)

Company: https://www.keypedia.com/companies/abl-manufacturing-llc/2eb0876d-0b50-41c6-a832-f3afd34bba43

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