Orca1

FDA inspection

Precision Herbs LLC: FDA inspection ending Jan 21, 2016

FDA inspection 959783 · Killbuck, OH

Key facts

Inspection ID 959783
Firm Precision Herbs LLC
FEI number 3006703597
Address 9804 Township Road 89
City Killbuck
State OH
ZIP 44637-9401
Fiscal year 2016
Inspection end date Jan 21, 2016
Project area Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance|Compliance: Medical Devices|Drug Quality Assurance
Product type Devices, Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

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

Other inspections at this establishment

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

Browse all FDA inspections