FDA inspection

RWM Technologies LLC: FDA inspection ending Dec 12, 2025

FDA inspection 1294946 · Chattanooga, TN

Key facts

Inspection ID 1294946
Firm RWM Technologies LLC
FEI number 3005940146
Address 3801 N Hawthorne St
City Chattanooga
State TN
ZIP 37406-1310
Fiscal year 2026
Inspection end date Dec 12, 2025
Project area Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices
Product type Drugs

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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