FDA inspection
PhotonX TherapeutX Inc.: FDA inspection ending Apr 4, 2017
FDA inspection 1014031 · No Action Indicated (NAI) · Oldsmar, FL
Key facts
| Inspection ID | 1014031 |
|---|---|
| Firm | PhotonX TherapeutX Inc. |
| FEI number | 3011422619 |
| Address | 640 Brooker Creek Blvd Ste 455 |
| City | Oldsmar |
| State | FL |
| ZIP | 34677-2934 |
| Fiscal year | 2017 |
| Inspection end date | Apr 4, 2017 |
| Classification | No Action Indicated (NAI) |
| Project area | Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch 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Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Product Evaluation: Med Devices|Product 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| Product type | Biologics, Devices, Drugs |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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