FDA inspection
Light Age, Inc.: FDA inspection ending Jul 27, 2009
FDA inspection 605641 · Somerset, NJ
Key facts
| Inspection ID | 605641 |
|---|---|
| Firm | Light Age, Inc. |
| FEI number | 2246844 |
| Address | 347 Elizabeth Ave Ste 106 |
| City | Somerset |
| State | NJ |
| ZIP | 08873-1123 |
| Fiscal year | 2009 |
| Inspection end date | Jul 27, 2009 |
| 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|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Rad Cntrl & Hlth Safety Act (RCHSA) Auth |
| Product type | Devices |
At a glance
- None 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