FDA inspection
MD Instruments Mfg. Co., Ltd.: FDA inspection ending Apr 13, 2023
FDA inspection 1202882 · Inashiki-Gun
Key facts
| Inspection ID | 1202882 |
|---|---|
| Firm | MD Instruments Mfg. Co., Ltd. |
| FEI number | 3013360312 |
| Address | 3262-3, Yoshiwara; Ami-Machi |
| City | Inashiki-Gun |
| Fiscal year | 2023 |
| Inspection end date | Apr 13, 2023 |
| Project area | Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) 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Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority|Radiation Control and Health Safety Act (RCHSA) Authority |
| Product type | Devices |
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
- 1–9 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