Crown Laboratories, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 1019820
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 1019820
- Address
- 349 Lafe Cox Drive, Johnson City, TN, 37604
Frequently asked questions
How many devices does CROWN LABORATORIES, INC. have in the registry?
The registry currently lists 2 devices for CROWN LABORATORIES, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list CROWN LABORATORIES, INC.'s devices?
Among its 2 most recently registered devices, CROWN LABORATORIES, INC. has devices listed in FDA GUDID (2 devices).
What are the newest devices from CROWN LABORATORIES, INC. in the registry?
The most recently registered devices listed for CROWN LABORATORIES, INC. include PanOxyl Antimicrobial Purifying Mist F83031 and PanOxyl Antimicrobial Purifying Mist F83062.