# FDA Inspection 820229 - OPMX, LLC - February 20, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/opmx-llc/e73e23d9-1cab-4277-808c-a5a9bb54b2d5
Source feed: FDA_Inspections

> FDA Inspection 820229 for OPMX, LLC on February 20, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 820229
- Company Name: OPMX, LLC
- Inspection Date: 2013-02-20
- Classification: No Action Indicated (NAI)
- Project Area: Unapproved and Misbranded Drugs
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

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Company: https://www.globalkeysolutions.net/companies/opmx-llc/3bb15278-e9e3-4a25-b3e8-3bc125fff8d8

Office: https://www.globalkeysolutions.net/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c